Canonical Allele Identifier: CA2190311942

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80180954C= , CM000677.2:g.80180954C=	GRCh38
NC_000015.9:g.80473296C= , CM000677.1:g.80473296C=	GRCh37
NC_000015.8:g.78260351C=	NCBI36
NG_012833.1:g.32956C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682012.1:n.1152-88C=
ENST00000561421.6:c.1063-88C= MANE Select	ENSP00000453347.2:n.1063-88C=
ENST00000646551.1:n.2677-88C=
ENST00000261755.9:c.1063-88C=	ENSP00000261755.5:n.1063-88C=
ENST00000407106.5:c.1063-88C=	ENSP00000385080.1:n.1063-88C=
ENST00000539156.5:c.853-88C=	ENSP00000454271.1:n.853-88C=
ENST00000559217.1:n.280-88C=
ENST00000561353.2:c.266-88C=
ENST00000561421.5:c.1063-88C=	ENSP00000453347.1:n.1063-88C=
NM_000137.2:c.1063-88C=	NP_000128.1:n.1063-88C=
XM_024449872.1:c.1063-88C=	XP_024305640.1:n.1063-88C=
NM_000137.4:c.1063-88C= MANE Select	NP_000128.1:n.1063-88C=
NM_001374377.1:c.1063-88C=	NP_001361306.1:n.1063-88C=
NM_001374380.1:c.1063-88C=	NP_001361309.1:n.1063-88C=