Canonical Allele Identifier: CA371120535

Gene: HGSNAT

Linked Data

• MyVariant Identifiers: chr8:g.43052861T>A (hg19) ; chr8:g.43197718T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43197718T>A , CM000670.2:g.43197718T>A	GRCh38
NC_000008.10:g.43052861T>A , CM000670.1:g.43052861T>A	GRCh37
NC_000008.9:g.43172018T>A	NCBI36
NG_009552.1:g.62270T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.1589T>A MANE Select	ENSP00000368965.4:p.Phe530Tyr
ENST00000379644.8:c.1589T>A	ENSP00000368965.4:p.Phe530Tyr
ENST00000519705.1:n.905T>A
ENST00000521576.1:c.740T>A	ENSP00000429029.1:p.Phe247Tyr
ENST00000523989.1:n.1902T>A
NM_152419.2:c.1589T>A	NP_689632.2:p.Phe530Tyr
XM_005273409.1:c.1700T>A	XP_005273466.1:p.Phe567Tyr
XM_005273410.1:c.1676T>A	XP_005273467.1:p.Phe559Tyr
XM_005273411.1:c.1508T>A	XP_005273468.1:p.Phe503Tyr
NM_001363227.1:c.1676T>A	NP_001350156.1:p.Phe559Tyr
NM_001363228.1:c.1397T>A	NP_001350157.1:p.Phe466Tyr
NM_001363229.1:c.725T>A	NP_001350158.1:p.Phe242Tyr
NM_152419.3:c.1589T>A MANE Select	NP_689632.2:p.Phe530Tyr
NM_001363227.2:c.1676T>A	NP_001350156.1:p.Phe559Tyr
NM_001363228.2:c.1397T>A	NP_001350157.1:p.Phe466Tyr
NM_001363229.2:c.725T>A	NP_001350158.1:p.Phe242Tyr