Canonical Allele Identifier: CA393619965

Gene: FAH

Linked Data

• ClinVar Variation Id: 2910382
• ClinVar RCV Id: RCV003634190
• MyVariant Identifiers: chr15:g.80460492G>A (hg19) ; chr15:g.80168150G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80168150G>A , CM000677.2:g.80168150G>A	GRCh38
NC_000015.9:g.80460492G>A , CM000677.1:g.80460492G>A	GRCh37
NC_000015.8:g.78247547G>A	NCBI36
NG_012833.1:g.20152G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.629G>A
ENST00000684569.1:n.598+1G>A
ENST00000561421.6:c.553+1G>A MANE Select	ENSP00000453347.2:n.553+1G>A
ENST00000646551.1:n.2180+1G>A
ENST00000261755.9:c.553+1G>A	ENSP00000261755.5:n.553+1G>A
ENST00000407106.5:c.553+1G>A	ENSP00000385080.1:n.553+1G>A
ENST00000539156.5:c.343+1G>A	ENSP00000454271.1:n.343+1G>A
ENST00000558514.1:n.99+1G>A
ENST00000558627.1:n.481+1G>A
ENST00000561421.5:c.553+1G>A	ENSP00000453347.1:n.553+1G>A
NM_000137.2:c.553+1G>A	NP_000128.1:n.553+1G>A
XM_024449872.1:c.553+1G>A	XP_024305640.1:n.553+1G>A
NM_000137.4:c.553+1G>A MANE Select	NP_000128.1:n.553+1G>A
NM_001374377.1:c.553+1G>A	NP_001361306.1:n.553+1G>A
NM_001374380.1:c.553+1G>A	NP_001361309.1:n.553+1G>A