Canonical Allele Identifier: CA1491668594

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125481563G= , CM000666.2:g.125481563G=	GRCh38
NC_000004.11:g.126402718G= , CM000666.1:g.126402718G=	GRCh37
NC_000004.10:g.126622168G=	NCBI36
NG_033865.1:g.170152G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.12647G= MANE Select	ENSP00000377862.4:p.Arg4216=
ENST00000674496.2:c.7418G=	ENSP00000501473.2:p.Arg2473=
ENST00000335110.5:c.7364G=	ENSP00000335169.5:p.Arg2455=
ENST00000394329.7:c.12641G=	ENSP00000377862.3:p.Arg4214=
NM_001291285.1:c.12647G=	NP_001278214.1:p.Arg4216=
NM_001291303.1:c.12647G=	NP_001278232.1:p.Arg4216=
NM_024582.4:c.12641G=	NP_078858.4:p.Arg4214=
XM_011532236.1:c.12647G=	XP_011530538.1:p.Arg4216=
XM_011532237.1:c.7418G=	XP_011530539.1:p.Arg2473=
XM_011532236.2:c.12647G=	XP_011530538.1:p.Arg4216=
XM_011532237.2:c.7418G=	XP_011530539.1:p.Arg2473=
NM_001291285.2:c.12647G=	NP_001278214.1:p.Arg4216=
NM_001291303.3:c.12647G= MANE Select	NP_001278232.1:p.Arg4216=
NM_024582.5:c.12641G=	NP_078858.4:p.Arg4214=
NM_001291285.3:c.12647G=	NP_001278214.1:p.Arg4216=
NM_024582.6:c.12641G=	NP_078858.4:p.Arg4214=