Canonical Allele Identifier: CA2190310559

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80180140T= , CM000677.2:g.80180140T=	GRCh38
NC_000015.9:g.80472482T= , CM000677.1:g.80472482T=	GRCh37
NC_000015.8:g.78259537T=	NCBI36
NG_012833.1:g.32142T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.1066T=
ENST00000561421.6:c.977T= MANE Select	ENSP00000453347.2:p.Met326=
ENST00000646551.1:n.2591T=
ENST00000261755.9:c.977T=	ENSP00000261755.5:p.Met326=
ENST00000407106.5:c.977T=	ENSP00000385080.1:p.Met326=
ENST00000539156.5:c.767T=	ENSP00000454271.1:p.Met256=
ENST00000559217.1:n.194T=
ENST00000561353.2:c.75T=
ENST00000561421.5:c.977T=	ENSP00000453347.1:p.Met326=
NM_000137.2:c.977T=	NP_000128.1:p.Met326=
XM_024449872.1:c.977T=	XP_024305640.1:p.Met326=
NM_000137.4:c.977T= MANE Select	NP_000128.1:p.Met326=
NM_001374377.1:c.977T=	NP_001361306.1:p.Met326=
NM_001374380.1:c.977T=	NP_001361309.1:p.Met326=