Canonical Allele Identifier: CA2190327562

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152870C= , CM000677.2:g.80152870C=	GRCh38
NC_000015.9:g.80445212C= , CM000677.1:g.80445212C=	GRCh37
NC_000015.8:g.78232267C=	NCBI36
NG_012833.1:g.4872C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.-185C=	ENSP00000507680.1:n.-185C=
ENST00000261755.9:c.-30+29C=	ENSP00000261755.5:n.-30+29C=
ENST00000407106.5:c.-65C=	ENSP00000385080.1:n.-65C=
ENST00000537726.5:n.53+29C=
ENST00000558022.5:c.-29-156C=	ENSP00000453152.1:n.-29-156C=
ENST00000558767.5:n.77C=
ENST00000561369.1:n.16C=
XM_024449872.1:c.-65C=	XP_024305640.1:n.-65C=
NM_001374377.1:c.-65C=	NP_001361306.1:n.-65C=
NM_001374380.1:c.-30+29C=	NP_001361309.1:n.-30+29C=