Canonical Allele Identifier: CA2629876382

Gene: FAH

Linked Data

• gnomAD v4: 15-80186108-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80186108T>G , CM000677.2:g.80186108T>G	GRCh38
NC_000015.9:g.80478450T>G , CM000677.1:g.80478450T>G	GRCh37
NC_000015.8:g.78265505T>G	NCBI36
NG_012833.1:g.38110T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682012.1:n.1270-22T>G
ENST00000561421.6:c.1181-22T>G MANE Select	ENSP00000453347.2:n.1181-22T>G
ENST00000646551.1:n.2795-22T>G
ENST00000261755.9:c.1181-22T>G	ENSP00000261755.5:n.1181-22T>G
ENST00000407106.5:c.1181-22T>G	ENSP00000385080.1:n.1181-22T>G
ENST00000539156.5:c.971-22T>G	ENSP00000454271.1:n.971-22T>G
ENST00000559217.1:n.398-22T>G
ENST00000561421.5:c.1181-22T>G	ENSP00000453347.1:n.1181-22T>G
NM_000137.2:c.1181-22T>G	NP_000128.1:n.1181-22T>G
XM_024449872.1:c.1181-22T>G	XP_024305640.1:n.1181-22T>G
NM_000137.4:c.1181-22T>G MANE Select	NP_000128.1:n.1181-22T>G
NM_001374377.1:c.1181-22T>G	NP_001361306.1:n.1181-22T>G
NM_001374380.1:c.1181-22T>G	NP_001361309.1:n.1181-22T>G