Description

SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 [Source:HGNC Symbol;Acc:18398]

Location
INSDC coordinates

chromosome:GRCh37:CM000666.1:95128762:95212443:1

Transcripts

This gene has 8 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDSGENCODE basic
SMARCAD1-005ENST000003590525017ENSP000003519471028Protein codingGenes and/or transcript that contains an open reading frame (ORF).CCDS47101-
SMARCAD1-002ENST000003542684912ENSP000003462171026Protein codingGenes and/or transcript that contains an open reading frame (ORF).CCDS3639YThe GENCODE Basic set includes all genes in the GENCODE gene set but only a subset of the transcripts.
SMARCAD1-001ENST000004578234649ENSP000004155761028Protein codingGenes and/or transcript that contains an open reading frame (ORF).CCDS47101YThe GENCODE Basic set includes all genes in the GENCODE gene set but only a subset of the transcripts.
SMARCAD1-006ENST000005094182348ENSP00000423286596Protein codingGenes and/or transcript that contains an open reading frame (ORF).CCDS58914YThe GENCODE Basic set includes all genes in the GENCODE gene set but only a subset of the transcripts.
SMARCAD1-007ENST000003949613778ENSP0000037841370Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. --
SMARCAD1-004ENST000005101052409ENSP00000424624244Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. --
SMARCAD1-009ENST00000506089554No protein product-Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.--
SMARCAD1-003ENST00000514232444No protein product-Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.--

Gene-based displays