Canonical Allele Identifier: CA1779762448

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43197673G= , CM000670.2:g.43197673G=	GRCh38
NC_000008.10:g.43052816G= , CM000670.1:g.43052816G=	GRCh37
NC_000008.9:g.43171973G=	NCBI36
NG_009552.1:g.62225G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.1544G= MANE Select	ENSP00000368965.4:p.Gly515=
ENST00000379644.8:c.1544G=	ENSP00000368965.4:p.Gly515=
ENST00000519705.1:n.860G=
ENST00000521576.1:c.695G=	ENSP00000429029.1:p.Gly232=
ENST00000523989.1:n.1857G=
NM_152419.2:c.1544G=	NP_689632.2:p.Gly515=
XM_005273409.1:c.1655G=	XP_005273466.1:p.Gly552=
XM_005273410.1:c.1631G=	XP_005273467.1:p.Gly544=
XM_005273411.1:c.1463G=	XP_005273468.1:p.Gly488=
NM_001363227.1:c.1631G=	NP_001350156.1:p.Gly544=
NM_001363228.1:c.1352G=	NP_001350157.1:p.Gly451=
NM_001363229.1:c.680G=	NP_001350158.1:p.Gly227=
NM_152419.3:c.1544G= MANE Select	NP_689632.2:p.Gly515=
NM_001363227.2:c.1631G=	NP_001350156.1:p.Gly544=
NM_001363228.2:c.1352G=	NP_001350157.1:p.Gly451=
NM_001363229.2:c.680G=	NP_001350158.1:p.Gly227=