Canonical Allele Identifier: CA2190333892

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80162273G= , CM000677.2:g.80162273G=	GRCh38
NC_000015.9:g.80454615G= , CM000677.1:g.80454615G=	GRCh37
NC_000015.8:g.78241670G=	NCBI36
NG_012833.1:g.14275G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.392G=	ENSP00000507680.1:p.Arg131=
ENST00000682012.1:n.467G=
ENST00000683593.1:n.2055G=
ENST00000684363.1:c.365-119G=	ENSP00000507314.1:n.365-119G=
ENST00000684569.1:n.437G=
ENST00000561421.6:c.392G= MANE Select	ENSP00000453347.2:p.Arg131=
ENST00000646551.1:n.1879G=
ENST00000261755.9:c.392G=	ENSP00000261755.5:p.Arg131=
ENST00000407106.5:c.392G=	ENSP00000385080.1:p.Arg131=
ENST00000537726.5:n.538G=
ENST00000539156.5:c.182G=	ENSP00000454271.1:p.Arg61=
ENST00000558022.5:c.392G=	ENSP00000453152.1:p.Arg131=
ENST00000558627.1:n.320G=
ENST00000558767.5:n.653G=
ENST00000561369.1:n.536G=
ENST00000561421.5:c.392G=	ENSP00000453347.1:p.Arg131=
NM_000137.2:c.392G=	NP_000128.1:p.Arg131=
XM_024449872.1:c.392G=	XP_024305640.1:p.Arg131=
NM_000137.4:c.392G= MANE Select	NP_000128.1:p.Arg131=
NM_001374377.1:c.392G=	NP_001361306.1:p.Arg131=
NM_001374380.1:c.392G=	NP_001361309.1:p.Arg131=