Canonical Allele Identifier: CA1491680375

Gene: FAT4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.125491556A= , CM000666.2:g.125491556A=	GRCh38
NC_000004.11:g.126412711A= , CM000666.1:g.126412711A=	GRCh37
NC_000004.10:g.126632161A=	NCBI36
NG_033865.1:g.180145A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394329.9:c.14740A= MANE Select	ENSP00000377862.4:p.Thr4914=
ENST00000674496.2:c.9511A=	ENSP00000501473.2:p.Thr3171=
ENST00000335110.5:c.9457A=	ENSP00000335169.5:p.Thr3153=
ENST00000394329.7:c.14734A=	ENSP00000377862.3:p.Thr4912=
NM_001291285.1:c.14737A=	NP_001278214.1:p.Thr4913=
NM_001291303.1:c.14740A=	NP_001278232.1:p.Thr4914=
NM_024582.4:c.14734A=	NP_078858.4:p.Thr4912=
XM_011532236.1:c.14740A=	XP_011530538.1:p.Thr4914=
XM_011532237.1:c.9511A=	XP_011530539.1:p.Thr3171=
XM_011532236.2:c.14740A=	XP_011530538.1:p.Thr4914=
XM_011532237.2:c.9511A=	XP_011530539.1:p.Thr3171=
NM_001291285.2:c.14737A=	NP_001278214.1:p.Thr4913=
NM_001291303.3:c.14740A= MANE Select	NP_001278232.1:p.Thr4914=
NM_024582.5:c.14734A=	NP_078858.4:p.Thr4912=
NM_001291285.3:c.14737A=	NP_001278214.1:p.Thr4913=
NM_024582.6:c.14734A=	NP_078858.4:p.Thr4912=