Canonical Allele Identifier: CA2629873090

Gene: FAH

Linked Data

• gnomAD v4: 15-80152980-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80152981del , CM000677.2:g.80152981del	GRCh38
NC_000015.9:g.80445323del , CM000677.1:g.80445323del	GRCh37
NC_000015.8:g.78232378del	NCBI36
NG_012833.1:g.4983del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.-74del	ENSP00000507680.1:n.-74del
ENST00000682012.1:n.2del
ENST00000261755.9:c.-29-45del	ENSP00000261755.5:n.-29-45del
ENST00000407106.5:c.-29-45del	ENSP00000385080.1:n.-29-45del
ENST00000537726.5:n.54-45del
ENST00000558022.5:c.-29-45del	ENSP00000453152.1:n.-29-45del
ENST00000558767.5:n.188del
ENST00000561369.1:n.52-45del
ENST00000561421.5:c.-74del	ENSP00000453347.1:n.-74del
NM_000137.2:c.-74del	NP_000128.1:n.-74del
XM_024449872.1:c.-29-45del	XP_024305640.1:n.-29-45del
NM_001374377.1:c.-29-45del	NP_001361306.1:n.-29-45del
NM_001374380.1:c.-29-45del	NP_001361309.1:n.-29-45del