Canonical Allele Identifier: CA358143766

Gene: FAT4

Linked Data

• COSMIC: COSM84867
• MyVariant Identifiers: chr4:g.126412799G>A (hg19) ; chr4:g.125491644G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491644G>A , CM000666.2:g.125491644G>A	GRCh38
NC_000004.11:g.126412799G>A , CM000666.1:g.126412799G>A	GRCh37
NC_000004.10:g.126632249G>A	NCBI36
NG_033865.1:g.180233G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.14828G>A MANE Select	ENSP00000377862.4:p.Gly4943Asp
ENST00000674496.2:c.9599G>A	ENSP00000501473.2:p.Gly3200Asp
ENST00000335110.5:c.9545G>A	ENSP00000335169.5:p.Gly3182Asp
ENST00000394329.7:c.14822G>A	ENSP00000377862.3:p.Gly4941Asp
NM_001291285.1:c.14825G>A	NP_001278214.1:p.Gly4942Asp
NM_001291303.1:c.14828G>A	NP_001278232.1:p.Gly4943Asp
NM_024582.4:c.14822G>A	NP_078858.4:p.Gly4941Asp
XM_011532236.1:c.14828G>A	XP_011530538.1:p.Gly4943Asp
XM_011532237.1:c.9599G>A	XP_011530539.1:p.Gly3200Asp
XM_011532236.2:c.14828G>A	XP_011530538.1:p.Gly4943Asp
XM_011532237.2:c.9599G>A	XP_011530539.1:p.Gly3200Asp
NM_001291285.2:c.14825G>A	NP_001278214.1:p.Gly4942Asp
NM_001291303.3:c.14828G>A MANE Select	NP_001278232.1:p.Gly4943Asp
NM_024582.5:c.14822G>A	NP_078858.4:p.Gly4941Asp
NM_001291285.3:c.14825G>A	NP_001278214.1:p.Gly4942Asp
NM_024582.6:c.14822G>A	NP_078858.4:p.Gly4941Asp