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Human (GRCh38.p14)
Description

structural maintenance of chromosomes 1B [Source:HGNC Symbol;Acc:HGNC:11112]

Gene Synonyms

BK268H5, SMC1L2

Location

Chromosome 22: 45,344,063-45,413,619 reverse strand.

GRCh38:CM000684.2

About this gene

This gene has 6 transcripts (splice variants), 205 orthologues, 7 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000357450.9SMC1B-20142331235aaENSP00000350036.4
 
Protein coding
CCDS43027Q8NDV3-3 NM_148674.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:5
ENST00001132656.1SMC1B-20642531235aaENSP00000808562.1
 
Protein coding
CCDS43027--Ensembl Canonical ExtendedGENCODE BasicAPPRIS P1
ENST00000877413.2SMC1B-20340551169aaENSP00000547472.1
 
Protein coding
--GENCODE Basic
ENST00000404354.4SMC1B-20240311161aaENSP00000385902.3
 
Protein coding
CCDS74876Q8NDV3-2 -GENCODE BasicTSL:1
ENST00000923332.2SMC1B-20437431065aaENSP00000593391.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00001099168.1SMC1B-20567780aaENSP00000768974.1
 
Nonsense mediated decay
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