Canonical Allele Identifier: CA2190338328

Gene: FAH

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80171973T= , CM000677.2:g.80171973T=	GRCh38
NC_000015.9:g.80464315T= , CM000677.1:g.80464315T=	GRCh37
NC_000015.8:g.78251370T=	NCBI36
NG_012833.1:g.23975T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.796-1041T=
ENST00000561421.6:c.607-176T= MANE Select	ENSP00000453347.2:n.607-176T=
ENST00000646551.1:n.2234-189T=
ENST00000261755.9:c.607-176T=	ENSP00000261755.5:n.607-176T=
ENST00000407106.5:c.607-176T=	ENSP00000385080.1:n.607-176T=
ENST00000539156.5:c.397-176T=	ENSP00000454271.1:n.397-176T=
ENST00000558627.1:n.535-176T=
ENST00000561421.5:c.607-176T=	ENSP00000453347.1:n.607-176T=
NM_000137.2:c.607-176T=	NP_000128.1:n.607-176T=
XM_024449872.1:c.607-176T=	XP_024305640.1:n.607-176T=
NM_000137.4:c.607-176T= MANE Select	NP_000128.1:n.607-176T=
NM_001374377.1:c.607-176T=	NP_001361306.1:n.607-176T=
NM_001374380.1:c.607-176T=	NP_001361309.1:n.607-176T=