Canonical Allele Identifier: CA1779762426

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43197634A= , CM000670.2:g.43197634A=	GRCh38
NC_000008.10:g.43052777A= , CM000670.1:g.43052777A=	GRCh37
NC_000008.9:g.43171934A=	NCBI36
NG_009552.1:g.62186A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.1543-38A= MANE Select	ENSP00000368965.4:n.1543-38A=
ENST00000379644.8:c.1543-38A=	ENSP00000368965.4:n.1543-38A=
ENST00000519705.1:n.859-38A=
ENST00000521576.1:c.694-38A=	ENSP00000429029.1:n.694-38A=
ENST00000523989.1:n.1818A=
NM_152419.2:c.1543-38A=	NP_689632.2:n.1543-38A=
XM_005273409.1:c.1654-38A=	XP_005273466.1:n.1654-38A=
XM_005273410.1:c.1630-38A=	XP_005273467.1:n.1630-38A=
XM_005273411.1:c.1462-38A=	XP_005273468.1:n.1462-38A=
NM_001363227.1:c.1630-38A=	NP_001350156.1:n.1630-38A=
NM_001363228.1:c.1351-38A=	NP_001350157.1:n.1351-38A=
NM_001363229.1:c.679-38A=	NP_001350158.1:n.679-38A=
NM_152419.3:c.1543-38A= MANE Select	NP_689632.2:n.1543-38A=
NM_001363227.2:c.1630-38A=	NP_001350156.1:n.1630-38A=
NM_001363228.2:c.1351-38A=	NP_001350157.1:n.1351-38A=
NM_001363229.2:c.679-38A=	NP_001350158.1:n.679-38A=