Canonical Allele Identifier: CA2190332739
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80159782G= , CM000677.2:g.80159782G= GRCh38
NC_000015.9:g.80452124G= , CM000677.1:g.80452124G= GRCh37
NC_000015.8:g.78239179G= NCBI36
NG_012833.1:g.11784G=

Transcript Alleles

HGVS Amino-acid change
ENST00000558767.6:c.219G= ENSP00000507680.1:p.Leu73=
ENST00000682012.1:n.294G=
ENST00000683593.1:n.96G=
ENST00000684363.1:c.219G= ENSP00000507314.1:p.Leu73=
ENST00000684569.1:n.264G=
ENST00000561421.6:c.219G= MANE Select ENSP00000453347.2:p.Leu73=
ENST00000646551.1:n.1706G=
ENST00000261755.9:c.219G= ENSP00000261755.5:p.Leu73=
ENST00000407106.5:c.219G= ENSP00000385080.1:p.Leu73=
ENST00000537726.5:n.301G=
ENST00000539156.5:c.9G= ENSP00000454271.1:p.Leu3=
ENST00000558022.5:c.219G= ENSP00000453152.1:p.Leu73=
ENST00000558767.5:n.480G=
ENST00000561369.1:n.299G=
ENST00000561421.5:c.219G= ENSP00000453347.1:p.Leu73=
NM_000137.2:c.219G= NP_000128.1:p.Leu73=
XM_024449872.1:c.219G= XP_024305640.1:p.Leu73=
NM_000137.4:c.219G= MANE Select NP_000128.1:p.Leu73=
NM_001374377.1:c.219G= NP_001361306.1:p.Leu73=
NM_001374380.1:c.219G= NP_001361309.1:p.Leu73=