Canonical Allele Identifier: CA2190333857
Gene: FAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80162183A= , CM000677.2:g.80162183A= GRCh38
NC_000015.9:g.80454525A= , CM000677.1:g.80454525A= GRCh37
NC_000015.8:g.78241580A= NCBI36
NG_012833.1:g.14185A=

Transcript Alleles

HGVS Amino-acid change
ENST00000558767.6:c.365-63A= ENSP00000507680.1:n.365-63A=
ENST00000682012.1:n.440-63A=
ENST00000683593.1:n.1965A=
ENST00000684363.1:c.365-209A= ENSP00000507314.1:n.365-209A=
ENST00000684569.1:n.410-63A=
ENST00000561421.6:c.365-63A= MANE Select ENSP00000453347.2:n.365-63A=
ENST00000646551.1:n.1852-63A=
ENST00000261755.9:c.365-63A= ENSP00000261755.5:n.365-63A=
ENST00000407106.5:c.365-63A= ENSP00000385080.1:n.365-63A=
ENST00000537726.5:n.511-63A=
ENST00000539156.5:c.155-63A= ENSP00000454271.1:n.155-63A=
ENST00000558022.5:c.365-63A= ENSP00000453152.1:n.365-63A=
ENST00000558627.1:n.293-63A=
ENST00000558767.5:n.626-63A=
ENST00000561369.1:n.509-63A=
ENST00000561421.5:c.365-63A= ENSP00000453347.1:n.365-63A=
NM_000137.2:c.365-63A= NP_000128.1:n.365-63A=
XM_024449872.1:c.365-63A= XP_024305640.1:n.365-63A=
NM_000137.4:c.365-63A= MANE Select NP_000128.1:n.365-63A=
NM_001374377.1:c.365-63A= NP_001361306.1:n.365-63A=
NM_001374380.1:c.365-63A= NP_001361309.1:n.365-63A=