Canonical Allele Identifier: CA1491680358

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491548C= , CM000666.2:g.125491548C=	GRCh38
NC_000004.11:g.126412703C= , CM000666.1:g.126412703C=	GRCh37
NC_000004.10:g.126632153C=	NCBI36
NG_033865.1:g.180137C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.14732C= MANE Select	ENSP00000377862.4:p.Ala4911=
ENST00000674496.2:c.9503C=	ENSP00000501473.2:p.Ala3168=
ENST00000335110.5:c.9449C=	ENSP00000335169.5:p.Ala3150=
ENST00000394329.7:c.14726C=	ENSP00000377862.3:p.Ala4909=
NM_001291285.1:c.14729C=	NP_001278214.1:p.Ala4910=
NM_001291303.1:c.14732C=	NP_001278232.1:p.Ala4911=
NM_024582.4:c.14726C=	NP_078858.4:p.Ala4909=
XM_011532236.1:c.14732C=	XP_011530538.1:p.Ala4911=
XM_011532237.1:c.9503C=	XP_011530539.1:p.Ala3168=
XM_011532236.2:c.14732C=	XP_011530538.1:p.Ala4911=
XM_011532237.2:c.9503C=	XP_011530539.1:p.Ala3168=
NM_001291285.2:c.14729C=	NP_001278214.1:p.Ala4910=
NM_001291303.3:c.14732C= MANE Select	NP_001278232.1:p.Ala4911=
NM_024582.5:c.14726C=	NP_078858.4:p.Ala4909=
NM_001291285.3:c.14729C=	NP_001278214.1:p.Ala4910=
NM_024582.6:c.14726C=	NP_078858.4:p.Ala4909=