Canonical Allele Identifier: CA2190338399
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80172156T= , CM000677.2:g.80172156T= GRCh38
NC_000015.9:g.80464498T= , CM000677.1:g.80464498T= GRCh37
NC_000015.8:g.78251553T= NCBI36
NG_012833.1:g.24158T=

Transcript Alleles

HGVS Amino-acid change
ENST00000682012.1:n.796-858T=
ENST00000561421.6:c.614T= MANE Select ENSP00000453347.2:p.Phe205=
ENST00000646551.1:n.2234-6T=
ENST00000261755.9:c.614T= ENSP00000261755.5:p.Phe205=
ENST00000407106.5:c.614T= ENSP00000385080.1:p.Phe205=
ENST00000539156.5:c.404T= ENSP00000454271.1:p.Phe135=
ENST00000558627.1:n.542T=
ENST00000561421.5:c.614T= ENSP00000453347.1:p.Phe205=
NM_000137.2:c.614T= NP_000128.1:p.Phe205=
XM_024449872.1:c.614T= XP_024305640.1:p.Phe205=
NM_000137.4:c.614T= MANE Select NP_000128.1:p.Phe205=
NM_001374377.1:c.614T= NP_001361306.1:p.Phe205=
NM_001374380.1:c.614T= NP_001361309.1:p.Phe205=