Canonical Allele Identifier: CA1491662385

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125468753G= , CM000666.2:g.125468753G=	GRCh38
NC_000004.11:g.126389908G= , CM000666.1:g.126389908G=	GRCh37
NC_000004.10:g.126609358G=	NCBI36
NG_033865.1:g.157342G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.12147G= MANE Select	ENSP00000377862.4:p.Lys4049=
ENST00000674496.2:c.6918G=	ENSP00000501473.2:p.Lys2306=
ENST00000335110.5:c.6930G=	ENSP00000335169.5:p.Lys2310=
ENST00000394329.7:c.12141G=	ENSP00000377862.3:p.Lys4047=
NM_001291285.1:c.12147G=	NP_001278214.1:p.Lys4049=
NM_001291303.1:c.12147G=	NP_001278232.1:p.Lys4049=
NM_024582.4:c.12141G=	NP_078858.4:p.Lys4047=
XM_011532236.1:c.12147G=	XP_011530538.1:p.Lys4049=
XM_011532237.1:c.6918G=	XP_011530539.1:p.Lys2306=
XM_011532236.2:c.12147G=	XP_011530538.1:p.Lys4049=
XM_011532237.2:c.6918G=	XP_011530539.1:p.Lys2306=
NM_001291285.2:c.12147G=	NP_001278214.1:p.Lys4049=
NM_001291303.3:c.12147G= MANE Select	NP_001278232.1:p.Lys4049=
NM_024582.5:c.12141G=	NP_078858.4:p.Lys4047=
NM_001291285.3:c.12147G=	NP_001278214.1:p.Lys4049=
NM_024582.6:c.12141G=	NP_078858.4:p.Lys4047=