Canonical Allele Identifier: CA371119744

Gene: HGSNAT

Linked Data

• MyVariant Identifiers: chr8:g.43047549C>A (hg19) ; chr8:g.43192406C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43192406C>A , CM000670.2:g.43192406C>A	GRCh38
NC_000008.10:g.43047549C>A , CM000670.1:g.43047549C>A	GRCh37
NC_000008.9:g.43166706C>A	NCBI36
NG_009552.1:g.56958C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.1353C>A MANE Select	ENSP00000368965.4:p.His451Gln
ENST00000379644.8:c.1353C>A	ENSP00000368965.4:p.His451Gln
ENST00000520678.1:n.286C>A
ENST00000521576.1:c.504C>A	ENSP00000429029.1:p.His168Gln
ENST00000524016.5:c.457C>A
NM_152419.2:c.1353C>A	NP_689632.2:p.His451Gln
XM_005273409.1:c.1353C>A	XP_005273466.1:p.His451Gln
XM_005273410.1:c.1353C>A	XP_005273467.1:p.His451Gln
XM_005273411.1:c.1161C>A	XP_005273468.1:p.His387Gln
XM_005273412.2:c.1353C>A	XP_005273469.1:p.His451Gln
NM_001363227.1:c.1353C>A	NP_001350156.1:p.His451Gln
NM_001363228.1:c.1161C>A	NP_001350157.1:p.His387Gln
NM_001363229.1:c.489C>A	NP_001350158.1:p.His163Gln
XM_005273412.4:c.1353C>A	XP_005273469.1:p.His451Gln
NM_152419.3:c.1353C>A MANE Select	NP_689632.2:p.His451Gln
NM_001363227.2:c.1353C>A	NP_001350156.1:p.His451Gln
NM_001363228.2:c.1161C>A	NP_001350157.1:p.His387Gln
NM_001363229.2:c.489C>A	NP_001350158.1:p.His163Gln