Canonical Allele Identifier: CA2190327662

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152929T= , CM000677.2:g.80152929T=	GRCh38
NC_000015.9:g.80445271T= , CM000677.1:g.80445271T=	GRCh37
NC_000015.8:g.78232326T=	NCBI36
NG_012833.1:g.4931T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.-126T=	ENSP00000507680.1:n.-126T=
ENST00000261755.9:c.-30+88T=	ENSP00000261755.5:n.-30+88T=
ENST00000407106.5:c.-30+24T=	ENSP00000385080.1:n.-30+24T=
ENST00000537726.5:n.53+88T=
ENST00000558022.5:c.-29-97T=	ENSP00000453152.1:n.-29-97T=
ENST00000558767.5:n.136T=
ENST00000561369.1:n.51+24T=
ENST00000561421.5:c.-126T=	ENSP00000453347.1:n.-126T=
NM_000137.2:c.-126T=	NP_000128.1:n.-126T=
XM_024449872.1:c.-30+24T=	XP_024305640.1:n.-30+24T=
NM_001374377.1:c.-30+24T=	NP_001361306.1:n.-30+24T=
NM_001374380.1:c.-30+88T=	NP_001361309.1:n.-30+88T=