Canonical Allele Identifier: CA2629874277

Gene: FAH

Linked Data

• gnomAD v4: 15-80180002-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80180002G>C , CM000677.2:g.80180002G>C	GRCh38
NC_000015.9:g.80472344G>C , CM000677.1:g.80472344G>C	GRCh37
NC_000015.8:g.78259399G>C	NCBI36
NG_012833.1:g.32004G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682012.1:n.1050-122G>C
ENST00000561421.6:c.961-122G>C MANE Select	ENSP00000453347.2:n.961-122G>C
ENST00000646551.1:n.2575-122G>C
ENST00000261755.9:c.961-122G>C	ENSP00000261755.5:n.961-122G>C
ENST00000407106.5:c.961-122G>C	ENSP00000385080.1:n.961-122G>C
ENST00000539156.5:c.751-122G>C	ENSP00000454271.1:n.751-122G>C
ENST00000559217.1:n.178-122G>C
ENST00000561353.2:c.59-122G>C
ENST00000561421.5:c.961-122G>C	ENSP00000453347.1:n.961-122G>C
NM_000137.2:c.961-122G>C	NP_000128.1:n.961-122G>C
XM_024449872.1:c.961-122G>C	XP_024305640.1:n.961-122G>C
NM_000137.4:c.961-122G>C MANE Select	NP_000128.1:n.961-122G>C
NM_001374377.1:c.961-122G>C	NP_001361306.1:n.961-122G>C
NM_001374380.1:c.961-122G>C	NP_001361309.1:n.961-122G>C