Canonical Allele Identifier: CA2190338398
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80172151T= , CM000677.2:g.80172151T= GRCh38
NC_000015.9:g.80464493T= , CM000677.1:g.80464493T= GRCh37
NC_000015.8:g.78251548T= NCBI36
NG_012833.1:g.24153T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682012.1:n.796-863T=
ENST00000561421.6:c.609T= MANE Select ENSP00000453347.2:p.Ala203=
ENST00000646551.1:n.2234-11T=
ENST00000261755.9:c.609T= ENSP00000261755.5:p.Ala203=
ENST00000407106.5:c.609T= ENSP00000385080.1:p.Ala203=
ENST00000539156.5:c.399T= ENSP00000454271.1:p.Ala133=
ENST00000558627.1:n.537T=
ENST00000561421.5:c.609T= ENSP00000453347.1:p.Ala203=
NM_000137.2:c.609T= NP_000128.1:p.Ala203=
XM_024449872.1:c.609T= XP_024305640.1:p.Ala203=
NM_000137.4:c.609T= MANE Select NP_000128.1:p.Ala203=
NM_001374377.1:c.609T= NP_001361306.1:p.Ala203=
NM_001374380.1:c.609T= NP_001361309.1:p.Ala203=