Canonical Allele Identifier: CA2190327796

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152980G= , CM000677.2:g.80152980G=	GRCh38
NC_000015.9:g.80445322G= , CM000677.1:g.80445322G=	GRCh37
NC_000015.8:g.78232377G=	NCBI36
NG_012833.1:g.4982G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000558767.6:c.-75G=	ENSP00000507680.1:n.-75G=
ENST00000682012.1:n.1G=
ENST00000261755.9:c.-29-46G=	ENSP00000261755.5:n.-29-46G=
ENST00000407106.5:c.-29-46G=	ENSP00000385080.1:n.-29-46G=
ENST00000537726.5:n.54-46G=
ENST00000558022.5:c.-29-46G=	ENSP00000453152.1:n.-29-46G=
ENST00000558767.5:n.187G=
ENST00000561369.1:n.52-46G=
ENST00000561421.5:c.-75G=	ENSP00000453347.1:n.-75G=
NM_000137.2:c.-75G=	NP_000128.1:n.-75G=
XM_024449872.1:c.-29-46G=	XP_024305640.1:n.-29-46G=
NM_001374377.1:c.-29-46G=	NP_001361306.1:n.-29-46G=
NM_001374380.1:c.-29-46G=	NP_001361309.1:n.-29-46G=