Canonical Allele Identifier: CA393621701

Gene: FAH

Linked Data

• MyVariant Identifiers: chr15:g.80472491A>T (hg19) ; chr15:g.80180149A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80180149A>T , CM000677.2:g.80180149A>T	GRCh38
NC_000015.9:g.80472491A>T , CM000677.1:g.80472491A>T	GRCh37
NC_000015.8:g.78259546A>T	NCBI36
NG_012833.1:g.32151A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.1075A>T
ENST00000561421.6:c.986A>T MANE Select	ENSP00000453347.2:p.Gln329Leu
ENST00000646551.1:n.2600A>T
ENST00000261755.9:c.986A>T	ENSP00000261755.5:p.Gln329Leu
ENST00000407106.5:c.986A>T	ENSP00000385080.1:p.Gln329Leu
ENST00000539156.5:c.776A>T	ENSP00000454271.1:p.Gln259Leu
ENST00000559217.1:n.203A>T
ENST00000561353.2:c.84A>T
ENST00000561421.5:c.986A>T	ENSP00000453347.1:p.Gln329Leu
NM_000137.2:c.986A>T	NP_000128.1:p.Gln329Leu
XM_024449872.1:c.986A>T	XP_024305640.1:p.Gln329Leu
NM_000137.4:c.986A>T MANE Select	NP_000128.1:p.Gln329Leu
NM_001374377.1:c.986A>T	NP_001361306.1:p.Gln329Leu
NM_001374380.1:c.986A>T	NP_001361309.1:p.Gln329Leu