Canonical Allele Identifier: CA371121310

Gene: HGSNAT

Linked Data

• MyVariant Identifiers: chr8:g.43054591A>G (hg19) ; chr8:g.43199448A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43199448A>G , CM000670.2:g.43199448A>G	GRCh38
NC_000008.10:g.43054591A>G , CM000670.1:g.43054591A>G	GRCh37
NC_000008.9:g.43173748A>G	NCBI36
NG_009552.1:g.64000A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.1787A>G MANE Select	ENSP00000368965.4:p.Gln596Arg
ENST00000379644.8:c.1787A>G	ENSP00000368965.4:p.Gln596Arg
ENST00000519705.1:n.1103A>G
ENST00000521576.1:c.938A>G	ENSP00000429029.1:p.Gln313Arg
NM_152419.2:c.1787A>G	NP_689632.2:p.Gln596Arg
XM_005273409.1:c.1898A>G	XP_005273466.1:p.Gln633Arg
XM_005273410.1:c.1874A>G	XP_005273467.1:p.Gln625Arg
XM_005273411.1:c.1706A>G	XP_005273468.1:p.Gln569Arg
NM_001363227.1:c.1874A>G	NP_001350156.1:p.Gln625Arg
NM_001363228.1:c.1595A>G	NP_001350157.1:p.Gln532Arg
NM_001363229.1:c.923A>G	NP_001350158.1:p.Gln308Arg
NM_152419.3:c.1787A>G MANE Select	NP_689632.2:p.Gln596Arg
NM_001363227.2:c.1874A>G	NP_001350156.1:p.Gln625Arg
NM_001363228.2:c.1595A>G	NP_001350157.1:p.Gln532Arg
NM_001363229.2:c.923A>G	NP_001350158.1:p.Gln308Arg