Canonical Allele Identifier: CA1491646821

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125434327A= , CM000666.2:g.125434327A=	GRCh38
NC_000004.11:g.126355482A= , CM000666.1:g.126355482A=	GRCh37
NC_000004.10:g.126574932A=	NCBI36
NG_033865.1:g.122916A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.7101A= MANE Select	ENSP00000377862.4:p.Lys2367=
ENST00000674496.2:c.1872A=	ENSP00000501473.2:p.Lys624=
ENST00000335110.5:c.1995A=	ENSP00000335169.5:p.Lys665=
ENST00000394329.7:c.7101A=	ENSP00000377862.3:p.Lys2367=
NM_001291285.1:c.7101A=	NP_001278214.1:p.Lys2367=
NM_001291303.1:c.7101A=	NP_001278232.1:p.Lys2367=
NM_024582.4:c.7101A=	NP_078858.4:p.Lys2367=
XM_011532236.1:c.7101A=	XP_011530538.1:p.Lys2367=
XM_011532237.1:c.1872A=	XP_011530539.1:p.Lys624=
XM_011532236.2:c.7101A=	XP_011530538.1:p.Lys2367=
XM_011532237.2:c.1872A=	XP_011530539.1:p.Lys624=
NM_001291285.2:c.7101A=	NP_001278214.1:p.Lys2367=
NM_001291303.3:c.7101A= MANE Select	NP_001278232.1:p.Lys2367=
NM_024582.5:c.7101A=	NP_078858.4:p.Lys2367=
NM_001291285.3:c.7101A=	NP_001278214.1:p.Lys2367=
NM_024582.6:c.7101A=	NP_078858.4:p.Lys2367=