Canonical Allele Identifier: CA1491599679

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125317377G= , CM000666.2:g.125317377G=	GRCh38
NC_000004.11:g.126238532G= , CM000666.1:g.126238532G=	GRCh37
NC_000004.10:g.126457982G=	NCBI36
NG_033865.1:g.5966G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394329.9:c.966G= MANE Select	ENSP00000377862.4:p.Thr322=
ENST00000674496.2:c.-55+1400G=	ENSP00000501473.2:n.-55+1400G=
ENST00000394329.7:c.966G=	ENSP00000377862.3:p.Thr322=
NM_001291285.1:c.966G=	NP_001278214.1:p.Thr322=
NM_001291303.1:c.966G=	NP_001278232.1:p.Thr322=
NM_024582.4:c.966G=	NP_078858.4:p.Thr322=
XM_011532236.1:c.966G=	XP_011530538.1:p.Thr322=
XM_011532237.1:c.-55+1400G=	XP_011530539.1:n.-55+1400G=
XM_011532236.2:c.966G=	XP_011530538.1:p.Thr322=
XM_011532237.2:c.-55+1400G=	XP_011530539.1:n.-55+1400G=
NM_001291285.2:c.966G=	NP_001278214.1:p.Thr322=
NM_001291303.3:c.966G= MANE Select	NP_001278232.1:p.Thr322=
NM_024582.5:c.966G=	NP_078858.4:p.Thr322=
NM_001291285.3:c.966G=	NP_001278214.1:p.Thr322=
NM_024582.6:c.966G=	NP_078858.4:p.Thr322=