Canonical Allele Identifier: CA1491680602

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491736C= , CM000666.2:g.125491736C=	GRCh38
NC_000004.11:g.126412891C= , CM000666.1:g.126412891C=	GRCh37
NC_000004.10:g.126632341C=	NCBI36
NG_033865.1:g.180325C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.14920C= MANE Select	ENSP00000377862.4:p.Pro4974=
ENST00000674496.2:c.9691C=	ENSP00000501473.2:p.Pro3231=
ENST00000335110.5:c.9637C=	ENSP00000335169.5:p.Pro3213=
ENST00000394329.7:c.14914C=	ENSP00000377862.3:p.Pro4972=
NM_001291285.1:c.14917C=	NP_001278214.1:p.Pro4973=
NM_001291303.1:c.14920C=	NP_001278232.1:p.Pro4974=
NM_024582.4:c.14914C=	NP_078858.4:p.Pro4972=
XM_011532236.1:c.14920C=	XP_011530538.1:p.Pro4974=
XM_011532237.1:c.9691C=	XP_011530539.1:p.Pro3231=
XM_011532236.2:c.14920C=	XP_011530538.1:p.Pro4974=
XM_011532237.2:c.9691C=	XP_011530539.1:p.Pro3231=
NM_001291285.2:c.14917C=	NP_001278214.1:p.Pro4973=
NM_001291303.3:c.14920C= MANE Select	NP_001278232.1:p.Pro4974=
NM_024582.5:c.14914C=	NP_078858.4:p.Pro4972=
NM_001291285.3:c.14917C=	NP_001278214.1:p.Pro4973=
NM_024582.6:c.14914C=	NP_078858.4:p.Pro4972=