Canonical Allele Identifier: CA2190336522

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80168106C= , CM000677.2:g.80168106C=	GRCh38
NC_000015.9:g.80460448C= , CM000677.1:g.80460448C=	GRCh37
NC_000015.8:g.78247503C=	NCBI36
NG_012833.1:g.20108C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.585C=
ENST00000684569.1:n.555C=
ENST00000561421.6:c.510C= MANE Select	ENSP00000453347.2:p.Gly170=
ENST00000646551.1:n.2137C=
ENST00000261755.9:c.510C=	ENSP00000261755.5:p.Gly170=
ENST00000407106.5:c.510C=	ENSP00000385080.1:p.Gly170=
ENST00000539156.5:c.300C=	ENSP00000454271.1:p.Gly100=
ENST00000558514.1:n.56C=
ENST00000558627.1:n.438C=
ENST00000561421.5:c.510C=	ENSP00000453347.1:p.Gly170=
NM_000137.2:c.510C=	NP_000128.1:p.Gly170=
XM_024449872.1:c.510C=	XP_024305640.1:p.Gly170=
NM_000137.4:c.510C= MANE Select	NP_000128.1:p.Gly170=
NM_001374377.1:c.510C=	NP_001361306.1:p.Gly170=
NM_001374380.1:c.510C=	NP_001361309.1:p.Gly170=