Canonical Allele Identifier: CA441373746

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125490247G>A , CM000666.2:g.125490247G>A	GRCh38
NC_000004.11:g.126411402G>A , CM000666.1:g.126411402G>A	GRCh37
NC_000004.10:g.126630852G>A	NCBI36
NG_033865.1:g.178836G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001291303.3:c.13431G>A MANE Select	NP_001278232.1:p.Gln4477=
ENST00000394329.9:c.13431G>A MANE Select	ENSP00000377862.4:p.Gln4477=
NM_001291285.1:c.13428G>A	NP_001278214.1:p.Gln4476=
NM_001291285.2:c.13428G>A	NP_001278214.1:p.Gln4476=
NM_001291285.3:c.13428G>A	NP_001278214.1:p.Gln4476=
NM_001291303.1:c.13431G>A	NP_001278232.1:p.Gln4477=
NM_024582.4:c.13425G>A	NP_078858.4:p.Gln4475=
NM_024582.5:c.13425G>A	NP_078858.4:p.Gln4475=
NM_024582.6:c.13425G>A	NP_078858.4:p.Gln4475=
ENST00000335110.5:c.8148G>A	ENSP00000335169.5:p.Gln2716=
ENST00000394329.7:c.13425G>A	ENSP00000377862.3:p.Gln4475=
ENST00000674496.2:c.8202G>A	ENSP00000501473.2:p.Gln2734=
XM_011532236.1:c.13431G>A	XP_011530538.1:p.Gln4477=
XM_011532236.2:c.13431G>A	XP_011530538.1:p.Gln4477=
XM_011532237.1:c.8202G>A	XP_011530539.1:p.Gln2734=
XM_011532237.2:c.8202G>A	XP_011530539.1:p.Gln2734=