Canonical Allele Identifier: CA2629875013
Gene: FAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80168004_80168013del , CM000677.2:g.80168004_80168013del GRCh38
NC_000015.9:g.80460346_80460355del , CM000677.1:g.80460346_80460355del GRCh37
NC_000015.8:g.78247401_78247410del NCBI36
NG_012833.1:g.20006_20015del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682012.1:n.531-48_531-39del
ENST00000684569.1:n.501-48_501-39del
ENST00000561421.6:c.456-48_456-39del MANE Select ENSP00000453347.2:n.456-48_456-39del
ENST00000646551.1:n.2083-48_2083-39del
ENST00000261755.9:c.456-48_456-39del ENSP00000261755.5:n.456-48_456-39del
ENST00000407106.5:c.456-48_456-39del ENSP00000385080.1:n.456-48_456-39del
ENST00000539156.5:c.246-48_246-39del ENSP00000454271.1:n.246-48_246-39del
ENST00000558022.5:c.456-48_456-39del ENSP00000453152.1:n.456-48_456-39del
ENST00000558627.1:n.384-48_384-39del
ENST00000561421.5:c.456-48_456-39del ENSP00000453347.1:n.456-48_456-39del
NM_000137.2:c.456-48_456-39del NP_000128.1:n.456-48_456-39del
XM_024449872.1:c.456-48_456-39del XP_024305640.1:n.456-48_456-39del
NM_000137.4:c.456-48_456-39del MANE Select NP_000128.1:n.456-48_456-39del
NM_001374377.1:c.456-48_456-39del NP_001361306.1:n.456-48_456-39del
NM_001374380.1:c.456-48_456-39del NP_001361309.1:n.456-48_456-39del