Canonical Allele Identifier: CA1491662342

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125468641T= , CM000666.2:g.125468641T=	GRCh38
NC_000004.11:g.126389796T= , CM000666.1:g.126389796T=	GRCh37
NC_000004.10:g.126609246T=	NCBI36
NG_033865.1:g.157230T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.12035T= MANE Select	ENSP00000377862.4:p.Leu4012=
ENST00000674496.2:c.6806T=	ENSP00000501473.2:p.Leu2269=
ENST00000335110.5:c.6818T=	ENSP00000335169.5:p.Leu2273=
ENST00000394329.7:c.12029T=	ENSP00000377862.3:p.Leu4010=
NM_001291285.1:c.12035T=	NP_001278214.1:p.Leu4012=
NM_001291303.1:c.12035T=	NP_001278232.1:p.Leu4012=
NM_024582.4:c.12029T=	NP_078858.4:p.Leu4010=
XM_011532236.1:c.12035T=	XP_011530538.1:p.Leu4012=
XM_011532237.1:c.6806T=	XP_011530539.1:p.Leu2269=
XM_011532236.2:c.12035T=	XP_011530538.1:p.Leu4012=
XM_011532237.2:c.6806T=	XP_011530539.1:p.Leu2269=
NM_001291285.2:c.12035T=	NP_001278214.1:p.Leu4012=
NM_001291303.3:c.12035T= MANE Select	NP_001278232.1:p.Leu4012=
NM_024582.5:c.12029T=	NP_078858.4:p.Leu4010=
NM_001291285.3:c.12035T=	NP_001278214.1:p.Leu4012=
NM_024582.6:c.12029T=	NP_078858.4:p.Leu4010=