Canonical Allele Identifier: CA3073298

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125449031A>T , CM000666.2:g.125449031A>T	GRCh38
NC_000004.11:g.126370186A>T , CM000666.1:g.126370186A>T	GRCh37
NC_000004.10:g.126589636A>T	NCBI36
NG_033865.1:g.137620A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001291303.3:c.8021A>T MANE Select	NP_001278232.1:p.Asp2674Val
ENST00000394329.9:c.8021A>T MANE Select	ENSP00000377862.4:p.Asp2674Val
NM_001291285.1:c.8021A>T	NP_001278214.1:p.Asp2674Val
NM_001291285.2:c.8021A>T	NP_001278214.1:p.Asp2674Val
NM_001291285.3:c.8021A>T	NP_001278214.1:p.Asp2674Val
NM_001291303.1:c.8021A>T	NP_001278232.1:p.Asp2674Val
NM_024582.4:c.8015A>T	NP_078858.4:p.Asp2672Val
NM_024582.5:c.8015A>T	NP_078858.4:p.Asp2672Val
NM_024582.6:c.8015A>T	NP_078858.4:p.Asp2672Val
ENST00000335110.5:c.2909A>T	ENSP00000335169.5:p.Asp970Val
ENST00000394329.7:c.8015A>T	ENSP00000377862.3:p.Asp2672Val
ENST00000674496.2:c.2792A>T	ENSP00000501473.2:p.Asp931Val
XM_011532236.1:c.8021A>T	XP_011530538.1:p.Asp2674Val
XM_011532236.2:c.8021A>T	XP_011530538.1:p.Asp2674Val
XM_011532237.1:c.2792A>T	XP_011530539.1:p.Asp931Val
XM_011532237.2:c.2792A>T	XP_011530539.1:p.Asp931Val