Canonical Allele Identifier: CA2190327855

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80153002C= , CM000677.2:g.80153002C=	GRCh38
NC_000015.9:g.80445344C= , CM000677.1:g.80445344C=	GRCh37
NC_000015.8:g.78232399C=	NCBI36
NG_012833.1:g.5004C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.-53C=	ENSP00000507680.1:n.-53C=
ENST00000682012.1:n.23C=
ENST00000561421.6:c.-53C= MANE Select	ENSP00000453347.2:n.-53C=
ENST00000261755.9:c.-29-24C=	ENSP00000261755.5:n.-29-24C=
ENST00000407106.5:c.-29-24C=	ENSP00000385080.1:n.-29-24C=
ENST00000537726.5:n.54-24C=
ENST00000558022.5:c.-29-24C=	ENSP00000453152.1:n.-29-24C=
ENST00000558767.5:n.209C=
ENST00000561369.1:n.52-24C=
ENST00000561421.5:c.-53C=	ENSP00000453347.1:n.-53C=
NM_000137.2:c.-53C=	NP_000128.1:n.-53C=
XM_024449872.1:c.-29-24C=	XP_024305640.1:n.-29-24C=
NM_000137.4:c.-53C= MANE Select	NP_000128.1:n.-53C=
NM_001374377.1:c.-29-24C=	NP_001361306.1:n.-29-24C=
NM_001374380.1:c.-29-24C=	NP_001361309.1:n.-29-24C=