Canonical Allele Identifier: CA971897231
Gene: FAH HGNC NCBI

Linked Data

dbSNP Id: rs2041130617

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80159681_80159684dup , CM000677.2:g.80159681_80159684dup GRCh38
NC_000015.9:g.80452023_80452026dup , CM000677.1:g.80452023_80452026dup GRCh37
NC_000015.8:g.78239078_78239081dup NCBI36
NG_012833.1:g.11683_11686dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000558767.6:c.193-75_193-72dup ENSP00000507680.1:n.193-75_193-72dup
ENST00000682012.1:n.268-75_268-72dup
ENST00000683593.1:n.70-75_70-72dup
ENST00000684363.1:c.193-75_193-72dup ENSP00000507314.1:n.193-75_193-72dup
ENST00000684569.1:n.238-75_238-72dup
ENST00000561421.6:c.193-75_193-72dup MANE Select ENSP00000453347.2:n.193-75_193-72dup
ENST00000646551.1:n.1680-75_1680-72dup
ENST00000261755.9:c.193-75_193-72dup ENSP00000261755.5:n.193-75_193-72dup
ENST00000407106.5:c.193-75_193-72dup ENSP00000385080.1:n.193-75_193-72dup
ENST00000537726.5:n.275-75_275-72dup
ENST00000539156.5:c.-18-75_-18-72dup ENSP00000454271.1:n.-18-75_-18-72dup
ENST00000558022.5:c.193-75_193-72dup ENSP00000453152.1:n.193-75_193-72dup
ENST00000558767.5:n.454-75_454-72dup
ENST00000561369.1:n.273-75_273-72dup
ENST00000561421.5:c.193-75_193-72dup ENSP00000453347.1:n.193-75_193-72dup
NM_000137.2:c.193-75_193-72dup NP_000128.1:n.193-75_193-72dup
XM_024449872.1:c.193-75_193-72dup XP_024305640.1:n.193-75_193-72dup
NM_000137.4:c.193-75_193-72dup MANE Select NP_000128.1:n.193-75_193-72dup
NM_001374377.1:c.193-75_193-72dup NP_001361306.1:n.193-75_193-72dup
NM_001374380.1:c.193-75_193-72dup NP_001361309.1:n.193-75_193-72dup