Canonical Allele Identifier: CA1491602611

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125318680A= , CM000666.2:g.125318680A=	GRCh38
NC_000004.11:g.126239835A= , CM000666.1:g.126239835A=	GRCh37
NC_000004.10:g.126459285A=	NCBI36
NG_033865.1:g.7269A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.2269A= MANE Select	ENSP00000377862.4:p.Thr757=
ENST00000674496.2:c.-55+2703A=	ENSP00000501473.2:n.-55+2703A=
ENST00000394329.7:c.2269A=	ENSP00000377862.3:p.Thr757=
NM_001291285.1:c.2269A=	NP_001278214.1:p.Thr757=
NM_001291303.1:c.2269A=	NP_001278232.1:p.Thr757=
NM_024582.4:c.2269A=	NP_078858.4:p.Thr757=
XM_011532236.1:c.2269A=	XP_011530538.1:p.Thr757=
XM_011532237.1:c.-55+2703A=	XP_011530539.1:n.-55+2703A=
XM_011532236.2:c.2269A=	XP_011530538.1:p.Thr757=
XM_011532237.2:c.-55+2703A=	XP_011530539.1:n.-55+2703A=
NM_001291285.2:c.2269A=	NP_001278214.1:p.Thr757=
NM_001291303.3:c.2269A= MANE Select	NP_001278232.1:p.Thr757=
NM_024582.5:c.2269A=	NP_078858.4:p.Thr757=
NM_001291285.3:c.2269A=	NP_001278214.1:p.Thr757=
NM_024582.6:c.2269A=	NP_078858.4:p.Thr757=