Canonical Allele Identifier: CA491682532

Gene: FAH

Linked Data

• MyVariant Identifiers: chr15:g.80460466C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80168124C>G , CM000677.2:g.80168124C>G	GRCh38
NC_000015.9:g.80460466C>G , CM000677.1:g.80460466C>G	GRCh37
NC_000015.8:g.78247521C>G	NCBI36
NG_012833.1:g.20126C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.603C>G
ENST00000684569.1:n.573C>G
ENST00000561421.6:c.528C>G MANE Select	ENSP00000453347.2:p.Pro176=
ENST00000646551.1:n.2155C>G
ENST00000261755.9:c.528C>G	ENSP00000261755.5:p.Pro176=
ENST00000407106.5:c.528C>G	ENSP00000385080.1:p.Pro176=
ENST00000539156.5:c.318C>G	ENSP00000454271.1:p.Pro106=
ENST00000558514.1:n.74C>G
ENST00000558627.1:n.456C>G
ENST00000561421.5:c.528C>G	ENSP00000453347.1:p.Pro176=
NM_000137.2:c.528C>G	NP_000128.1:p.Pro176=
XM_024449872.1:c.528C>G	XP_024305640.1:p.Pro176=
NM_000137.4:c.528C>G MANE Select	NP_000128.1:p.Pro176=
NM_001374377.1:c.528C>G	NP_001361306.1:p.Pro176=
NM_001374380.1:c.528C>G	NP_001361309.1:p.Pro176=