Canonical Allele Identifier: CA1779777518

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43199494G= , CM000670.2:g.43199494G=	GRCh38
NC_000008.10:g.43054637G= , CM000670.1:g.43054637G=	GRCh37
NC_000008.9:g.43173794G=	NCBI36
NG_009552.1:g.64046G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.1833G= MANE Select	ENSP00000368965.4:p.Gln611=
ENST00000379644.8:c.1833G=	ENSP00000368965.4:p.Gln611=
ENST00000519705.1:n.1149G=
ENST00000521576.1:c.984G=	ENSP00000429029.1:p.Gln328=
NM_152419.2:c.1833G=	NP_689632.2:p.Gln611=
XM_005273409.1:c.1944G=	XP_005273466.1:p.Gln648=
XM_005273410.1:c.1920G=	XP_005273467.1:p.Gln640=
XM_005273411.1:c.1752G=	XP_005273468.1:p.Gln584=
NM_001363227.1:c.1920G=	NP_001350156.1:p.Gln640=
NM_001363228.1:c.1641G=	NP_001350157.1:p.Gln547=
NM_001363229.1:c.969G=	NP_001350158.1:p.Gln323=
NM_152419.3:c.1833G= MANE Select	NP_689632.2:p.Gln611=
NM_001363227.2:c.1920G=	NP_001350156.1:p.Gln640=
NM_001363228.2:c.1641G=	NP_001350157.1:p.Gln547=
NM_001363229.2:c.969G=	NP_001350158.1:p.Gln323=