Canonical Allele Identifier: CA2575861041

Gene: FAH

Linked Data

• gnomAD v4: 15-80177486-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80177486C>A , CM000677.2:g.80177486C>A	GRCh38
NC_000015.9:g.80469828C>A , CM000677.1:g.80469828C>A	GRCh37
NC_000015.8:g.78256883C>A	NCBI36
NG_012833.1:g.29488C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682012.1:n.1003-51C>A
ENST00000561421.6:c.914-51C>A MANE Select	ENSP00000453347.2:n.914-51C>A
ENST00000646551.1:n.2528-51C>A
ENST00000261755.9:c.914-51C>A	ENSP00000261755.5:n.914-51C>A
ENST00000407106.5:c.914-51C>A	ENSP00000385080.1:n.914-51C>A
ENST00000539156.5:c.704-51C>A	ENSP00000454271.1:n.704-51C>A
ENST00000559217.1:n.80C>A
ENST00000561353.2:c.12-51C>A
ENST00000561421.5:c.914-51C>A	ENSP00000453347.1:n.914-51C>A
NM_000137.2:c.914-51C>A	NP_000128.1:n.914-51C>A
XM_024449872.1:c.914-51C>A	XP_024305640.1:n.914-51C>A
NM_000137.4:c.914-51C>A MANE Select	NP_000128.1:n.914-51C>A
NM_001374377.1:c.914-51C>A	NP_001361306.1:n.914-51C>A
NM_001374380.1:c.914-51C>A	NP_001361309.1:n.914-51C>A