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Human (GRCh38.p14)
Description

coagulation factor X [Source:HGNC Symbol;Acc:HGNC:3528]

Location

Chromosome 13: 113,122,788-113,149,531 forward strand.

GRCh38:CM000675.2

About this gene

This gene has 10 transcripts (splice variants), 241 orthologues, 16 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000375559.8F10-2021536488aaENSP00000364709.3
 
Protein coding
CCDS9530P00742 Q5JVE7 NM_000504.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000858582.1F10-2091544491aaENSP00000528641.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000858583.1F10-2101526493aaENSP00000528642.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000375551.7F10-2011509332aaENSP00000364701.3
 
Protein coding
CCDS81783Q5JVE8 -GENCODE BasicTSL:1
ENST00000409306.5F10-2031450334aaENSP00000387092.1
 
Protein coding
B7ZBK1 -GENCODE BasicTSL:3
ENST00000858581.1F10-2081417444aaENSP00000528640.1
 
Protein coding
--GENCODE Basic
ENST00000410083.6F10-2041211130aaENSP00000386320.2
 
Nonsense mediated decay
F8WBM7 -TSL:1
ENST00000483537.1F10-206564No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000477269.5F10-205907No protein-
 
Retained intron
--TSL:1
ENST00000498455.1F10-207849No protein-
 
Retained intron
--TSL:2