Canonical Allele Identifier: CA393621656

Gene: FAH

Linked Data

• MyVariant Identifiers: chr15:g.80472472T>A (hg19) ; chr15:g.80180130T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80180130T>A , CM000677.2:g.80180130T>A	GRCh38
NC_000015.9:g.80472472T>A , CM000677.1:g.80472472T>A	GRCh37
NC_000015.8:g.78259527T>A	NCBI36
NG_012833.1:g.32132T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682012.1:n.1056T>A
ENST00000561421.6:c.967T>A MANE Select	ENSP00000453347.2:p.Tyr323Asn
ENST00000646551.1:n.2581T>A
ENST00000261755.9:c.967T>A	ENSP00000261755.5:p.Tyr323Asn
ENST00000407106.5:c.967T>A	ENSP00000385080.1:p.Tyr323Asn
ENST00000539156.5:c.757T>A	ENSP00000454271.1:p.Tyr253Asn
ENST00000559217.1:n.184T>A
ENST00000561353.2:c.65T>A
ENST00000561421.5:c.967T>A	ENSP00000453347.1:p.Tyr323Asn
NM_000137.2:c.967T>A	NP_000128.1:p.Tyr323Asn
XM_024449872.1:c.967T>A	XP_024305640.1:p.Tyr323Asn
NM_000137.4:c.967T>A MANE Select	NP_000128.1:p.Tyr323Asn
NM_001374377.1:c.967T>A	NP_001361306.1:p.Tyr323Asn
NM_001374380.1:c.967T>A	NP_001361309.1:p.Tyr323Asn