Canonical Allele Identifier: CA1491654917

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125446299G= , CM000666.2:g.125446299G=	GRCh38
NC_000004.11:g.126367454G= , CM000666.1:g.126367454G=	GRCh37
NC_000004.10:g.126586904G=	NCBI36
NG_033865.1:g.134888G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.7206G= MANE Select	ENSP00000377862.4:p.Arg2402=
ENST00000674496.2:c.1977G=	ENSP00000501473.2:p.Arg659=
ENST00000335110.5:c.2094G=	ENSP00000335169.5:p.Arg698=
ENST00000394329.7:c.7200G=	ENSP00000377862.3:p.Arg2400=
ENST00000509444.1:n.189G=
NM_001291285.1:c.7206G=	NP_001278214.1:p.Arg2402=
NM_001291303.1:c.7206G=	NP_001278232.1:p.Arg2402=
NM_024582.4:c.7200G=	NP_078858.4:p.Arg2400=
XM_011532236.1:c.7206G=	XP_011530538.1:p.Arg2402=
XM_011532237.1:c.1977G=	XP_011530539.1:p.Arg659=
XM_011532236.2:c.7206G=	XP_011530538.1:p.Arg2402=
XM_011532237.2:c.1977G=	XP_011530539.1:p.Arg659=
NM_001291285.2:c.7206G=	NP_001278214.1:p.Arg2402=
NM_001291303.3:c.7206G= MANE Select	NP_001278232.1:p.Arg2402=
NM_024582.5:c.7200G=	NP_078858.4:p.Arg2400=
NM_001291285.3:c.7206G=	NP_001278214.1:p.Arg2402=
NM_024582.6:c.7200G=	NP_078858.4:p.Arg2400=