Canonical Allele Identifier: CA2190332771

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80159851C= , CM000677.2:g.80159851C=	GRCh38
NC_000015.9:g.80452193C= , CM000677.1:g.80452193C=	GRCh37
NC_000015.8:g.78239248C=	NCBI36
NG_012833.1:g.11853C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.288C=	ENSP00000507680.1:p.Leu96=
ENST00000682012.1:n.363C=
ENST00000683593.1:n.165C=
ENST00000684363.1:c.288C=	ENSP00000507314.1:p.Leu96=
ENST00000684569.1:n.333C=
ENST00000561421.6:c.288C= MANE Select	ENSP00000453347.2:p.Leu96=
ENST00000646551.1:n.1775C=
ENST00000261755.9:c.288C=	ENSP00000261755.5:p.Leu96=
ENST00000407106.5:c.288C=	ENSP00000385080.1:p.Leu96=
ENST00000537726.5:n.370C=
ENST00000539156.5:c.78C=	ENSP00000454271.1:p.Leu26=
ENST00000558022.5:c.288C=	ENSP00000453152.1:p.Leu96=
ENST00000558767.5:n.549C=
ENST00000561369.1:n.368C=
ENST00000561421.5:c.288C=	ENSP00000453347.1:p.Leu96=
NM_000137.2:c.288C=	NP_000128.1:p.Leu96=
XM_024449872.1:c.288C=	XP_024305640.1:p.Leu96=
NM_000137.4:c.288C= MANE Select	NP_000128.1:p.Leu96=
NM_001374377.1:c.288C=	NP_001361306.1:p.Leu96=
NM_001374380.1:c.288C=	NP_001361309.1:p.Leu96=