Canonical Allele Identifier: CA2629873237
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80153214_80153215insGTGGAGTGGAATGGA , CM000677.2:g.80153214_80153215insGTGGAGTGGAATGGA GRCh38
NC_000015.9:g.80445556_80445557insGTGGAGTGGAATGGA , CM000677.1:g.80445556_80445557insGTGGAGTGGAATGGA GRCh37
NC_000015.8:g.78232611_78232612insGTGGAGTGGAATGGA NCBI36
NG_012833.1:g.5216_5217insGTGGAGTGGAATGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000558767.6:c.81+79_81+80insGTGGAGTGGAATGGA ENSP00000507680.1:n.81+79_81+80insGTGGAGTGGAATGGA
ENST00000682012.1:n.156+79_156+80insGTGGAGTGGAATGGA
ENST00000684363.1:c.81+79_81+80insGTGGAGTGGAATGGA ENSP00000507314.1:n.81+79_81+80insGTGGAGTGGAATGGA
ENST00000684569.1:n.126+79_126+80insGTGGAGTGGAATGGA
ENST00000561421.6:c.81+79_81+80insGTGGAGTGGAATGGA MANE Select ENSP00000453347.2:n.81+79_81+80insGTGGAGTGGAATGGA
ENST00000261755.9:c.81+79_81+80insGTGGAGTGGAATGGA ENSP00000261755.5:n.81+79_81+80insGTGGAGTGGAATGGA
ENST00000407106.5:c.81+79_81+80insGTGGAGTGGAATGGA ENSP00000385080.1:n.81+79_81+80insGTGGAGTGGAATGGA
ENST00000537726.5:n.163+79_163+80insGTGGAGTGGAATGGA
ENST00000558022.5:c.81+79_81+80insGTGGAGTGGAATGGA ENSP00000453152.1:n.81+79_81+80insGTGGAGTGGAATGGA
ENST00000558767.5:n.342+79_342+80insGTGGAGTGGAATGGA
ENST00000561369.1:n.161+79_161+80insGTGGAGTGGAATGGA
ENST00000561421.5:c.81+79_81+80insGTGGAGTGGAATGGA ENSP00000453347.1:n.81+79_81+80insGTGGAGTGGAATGGA
NM_000137.2:c.81+79_81+80insGTGGAGTGGAATGGA NP_000128.1:n.81+79_81+80insGTGGAGTGGAATGGA
XM_024449872.1:c.81+79_81+80insGTGGAGTGGAATGGA XP_024305640.1:n.81+79_81+80insGTGGAGTGGAATGGA
NM_000137.4:c.81+79_81+80insGTGGAGTGGAATGGA MANE Select NP_000128.1:n.81+79_81+80insGTGGAGTGGAATGGA
NM_001374377.1:c.81+79_81+80insGTGGAGTGGAATGGA NP_001361306.1:n.81+79_81+80insGTGGAGTGGAATGGA
NM_001374380.1:c.81+79_81+80insGTGGAGTGGAATGGA NP_001361309.1:n.81+79_81+80insGTGGAGTGGAATGGA