Canonical Allele Identifier: CA1491662367

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125468706G= , CM000666.2:g.125468706G=	GRCh38
NC_000004.11:g.126389861G= , CM000666.1:g.126389861G=	GRCh37
NC_000004.10:g.126609311G=	NCBI36
NG_033865.1:g.157295G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.12100G= MANE Select	ENSP00000377862.4:p.Glu4034=
ENST00000674496.2:c.6871G=	ENSP00000501473.2:p.Glu2291=
ENST00000335110.5:c.6883G=	ENSP00000335169.5:p.Glu2295=
ENST00000394329.7:c.12094G=	ENSP00000377862.3:p.Glu4032=
NM_001291285.1:c.12100G=	NP_001278214.1:p.Glu4034=
NM_001291303.1:c.12100G=	NP_001278232.1:p.Glu4034=
NM_024582.4:c.12094G=	NP_078858.4:p.Glu4032=
XM_011532236.1:c.12100G=	XP_011530538.1:p.Glu4034=
XM_011532237.1:c.6871G=	XP_011530539.1:p.Glu2291=
XM_011532236.2:c.12100G=	XP_011530538.1:p.Glu4034=
XM_011532237.2:c.6871G=	XP_011530539.1:p.Glu2291=
NM_001291285.2:c.12100G=	NP_001278214.1:p.Glu4034=
NM_001291303.3:c.12100G= MANE Select	NP_001278232.1:p.Glu4034=
NM_024582.5:c.12094G=	NP_078858.4:p.Glu4032=
NM_001291285.3:c.12100G=	NP_001278214.1:p.Glu4034=
NM_024582.6:c.12094G=	NP_078858.4:p.Glu4032=