Canonical Allele Identifier: CA1491662408

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125468804C= , CM000666.2:g.125468804C=	GRCh38
NC_000004.11:g.126389959C= , CM000666.1:g.126389959C=	GRCh37
NC_000004.10:g.126609409C=	NCBI36
NG_033865.1:g.157393C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.12198C= MANE Select	ENSP00000377862.4:p.Ala4066=
ENST00000674496.2:c.6969C=	ENSP00000501473.2:p.Ala2323=
ENST00000335110.5:c.6981C=	ENSP00000335169.5:p.Ala2327=
ENST00000394329.7:c.12192C=	ENSP00000377862.3:p.Ala4064=
NM_001291285.1:c.12198C=	NP_001278214.1:p.Ala4066=
NM_001291303.1:c.12198C=	NP_001278232.1:p.Ala4066=
NM_024582.4:c.12192C=	NP_078858.4:p.Ala4064=
XM_011532236.1:c.12198C=	XP_011530538.1:p.Ala4066=
XM_011532237.1:c.6969C=	XP_011530539.1:p.Ala2323=
XM_011532236.2:c.12198C=	XP_011530538.1:p.Ala4066=
XM_011532237.2:c.6969C=	XP_011530539.1:p.Ala2323=
NM_001291285.2:c.12198C=	NP_001278214.1:p.Ala4066=
NM_001291303.3:c.12198C= MANE Select	NP_001278232.1:p.Ala4066=
NM_024582.5:c.12192C=	NP_078858.4:p.Ala4064=
NM_001291285.3:c.12198C=	NP_001278214.1:p.Ala4066=
NM_024582.6:c.12192C=	NP_078858.4:p.Ala4064=