Canonical Allele Identifier: CA2190327888

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80153011C= , CM000677.2:g.80153011C=	GRCh38
NC_000015.9:g.80445353C= , CM000677.1:g.80445353C=	GRCh37
NC_000015.8:g.78232408C=	NCBI36
NG_012833.1:g.5013C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.-44C=	ENSP00000507680.1:n.-44C=
ENST00000682012.1:n.32C=
ENST00000684569.1:n.2C=
ENST00000561421.6:c.-44C= MANE Select	ENSP00000453347.2:n.-44C=
ENST00000261755.9:c.-29-15C=	ENSP00000261755.5:n.-29-15C=
ENST00000407106.5:c.-29-15C=	ENSP00000385080.1:n.-29-15C=
ENST00000537726.5:n.54-15C=
ENST00000558022.5:c.-29-15C=	ENSP00000453152.1:n.-29-15C=
ENST00000558767.5:n.218C=
ENST00000561369.1:n.52-15C=
ENST00000561421.5:c.-44C=	ENSP00000453347.1:n.-44C=
NM_000137.2:c.-44C=	NP_000128.1:n.-44C=
XM_024449872.1:c.-29-15C=	XP_024305640.1:n.-29-15C=
NM_000137.4:c.-44C= MANE Select	NP_000128.1:n.-44C=
NM_001374377.1:c.-29-15C=	NP_001361306.1:n.-29-15C=
NM_001374380.1:c.-29-15C=	NP_001361309.1:n.-29-15C=