Canonical Allele Identifier: CA2629872898
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80152857_80152955del , CM000677.2:g.80152857_80152955del GRCh38
NC_000015.9:g.80445199_80445297del , CM000677.1:g.80445199_80445297del GRCh37
NC_000015.8:g.78232254_78232352del NCBI36
NG_012833.1:g.4859_4957del

Transcript Alleles

HGVS Amino-acid Change
ENST00000558767.6:c.-198_-100del ENSP00000507680.1:n.-198_-100del
ENST00000261755.9:c.-30+16_-29-71del ENSP00000261755.5:n.-30+16_-29-71del
ENST00000407106.5:c.-78_-30+50del
ENST00000537726.5:n.53+16_54-71del
ENST00000558022.5:c.-29-169_-29-71del ENSP00000453152.1:n.-29-169_-29-71del
ENST00000558767.5:n.64_162del
XM_024449872.1:c.-78_-30+50del
NM_001374377.1:c.-78_-30+50del
NM_001374380.1:c.-30+16_-29-71del NP_001361309.1:n.-30+16_-29-71del