Canonical Allele Identifier: CA2629873142

Gene: FAH

Linked Data

• gnomAD v4: 15-80153044-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80153044T>G , CM000677.2:g.80153044T>G	GRCh38
NC_000015.9:g.80445386T>G , CM000677.1:g.80445386T>G	GRCh37
NC_000015.8:g.78232441T>G	NCBI36
NG_012833.1:g.5046T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.-11T>G	ENSP00000507680.1:n.-11T>G
ENST00000682012.1:n.65T>G
ENST00000684569.1:n.35T>G
ENST00000561421.6:c.-11T>G MANE Select	ENSP00000453347.2:n.-11T>G
ENST00000261755.9:c.-11T>G	ENSP00000261755.5:n.-11T>G
ENST00000407106.5:c.-11T>G	ENSP00000385080.1:n.-11T>G
ENST00000537726.5:n.72T>G
ENST00000558022.5:c.-11T>G	ENSP00000453152.1:n.-11T>G
ENST00000558767.5:n.251T>G
ENST00000561369.1:n.70T>G
ENST00000561421.5:c.-11T>G	ENSP00000453347.1:n.-11T>G
NM_000137.2:c.-11T>G	NP_000128.1:n.-11T>G
XM_024449872.1:c.-11T>G	XP_024305640.1:n.-11T>G
NM_000137.4:c.-11T>G MANE Select	NP_000128.1:n.-11T>G
NM_001374377.1:c.-11T>G	NP_001361306.1:n.-11T>G
NM_001374380.1:c.-11T>G	NP_001361309.1:n.-11T>G