Canonical Allele Identifier: CA393621702

Gene: FAH

Linked Data

• MyVariant Identifiers: chr15:g.80472492G>C (hg19) ; chr15:g.80180150G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80180150G>C , CM000677.2:g.80180150G>C	GRCh38
NC_000015.9:g.80472492G>C , CM000677.1:g.80472492G>C	GRCh37
NC_000015.8:g.78259547G>C	NCBI36
NG_012833.1:g.32152G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.1076G>C
ENST00000561421.6:c.987G>C MANE Select	ENSP00000453347.2:p.Gln329His
ENST00000646551.1:n.2601G>C
ENST00000261755.9:c.987G>C	ENSP00000261755.5:p.Gln329His
ENST00000407106.5:c.987G>C	ENSP00000385080.1:p.Gln329His
ENST00000539156.5:c.777G>C	ENSP00000454271.1:p.Gln259His
ENST00000559217.1:n.204G>C
ENST00000561353.2:c.85G>C
ENST00000561421.5:c.987G>C	ENSP00000453347.1:p.Gln329His
NM_000137.2:c.987G>C	NP_000128.1:p.Gln329His
XM_024449872.1:c.987G>C	XP_024305640.1:p.Gln329His
NM_000137.4:c.987G>C MANE Select	NP_000128.1:p.Gln329His
NM_001374377.1:c.987G>C	NP_001361306.1:p.Gln329His
NM_001374380.1:c.987G>C	NP_001361309.1:p.Gln329His