Canonical Allele Identifier: CA393619045

Gene: FAH

Linked Data

• gnomAD v4: 15-80159841-A-G
• MyVariant Identifiers: chr15:g.80452183A>G (hg19) ; chr15:g.80159841A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80159841A>G , CM000677.2:g.80159841A>G	GRCh38
NC_000015.9:g.80452183A>G , CM000677.1:g.80452183A>G	GRCh37
NC_000015.8:g.78239238A>G	NCBI36
NG_012833.1:g.11843A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558767.6:c.278A>G	ENSP00000507680.1:p.Gln93Arg
ENST00000682012.1:n.353A>G
ENST00000683593.1:n.155A>G
ENST00000684363.1:c.278A>G	ENSP00000507314.1:p.Gln93Arg
ENST00000684569.1:n.323A>G
ENST00000561421.6:c.278A>G MANE Select	ENSP00000453347.2:p.Gln93Arg
ENST00000646551.1:n.1765A>G
ENST00000261755.9:c.278A>G	ENSP00000261755.5:p.Gln93Arg
ENST00000407106.5:c.278A>G	ENSP00000385080.1:p.Gln93Arg
ENST00000537726.5:n.360A>G
ENST00000539156.5:c.68A>G	ENSP00000454271.1:p.Gln23Arg
ENST00000558022.5:c.278A>G	ENSP00000453152.1:p.Gln93Arg
ENST00000558767.5:n.539A>G
ENST00000561369.1:n.358A>G
ENST00000561421.5:c.278A>G	ENSP00000453347.1:p.Gln93Arg
NM_000137.2:c.278A>G	NP_000128.1:p.Gln93Arg
XM_024449872.1:c.278A>G	XP_024305640.1:p.Gln93Arg
NM_000137.4:c.278A>G MANE Select	NP_000128.1:p.Gln93Arg
NM_001374377.1:c.278A>G	NP_001361306.1:p.Gln93Arg
NM_001374380.1:c.278A>G	NP_001361309.1:p.Gln93Arg