Canonical Allele Identifier: CA1779762421

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43197621T= , CM000670.2:g.43197621T=	GRCh38
NC_000008.10:g.43052764T= , CM000670.1:g.43052764T=	GRCh37
NC_000008.9:g.43171921T=	NCBI36
NG_009552.1:g.62173T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.1543-51T= MANE Select	ENSP00000368965.4:n.1543-51T=
ENST00000379644.8:c.1543-51T=	ENSP00000368965.4:n.1543-51T=
ENST00000519705.1:n.859-51T=
ENST00000521576.1:c.694-51T=	ENSP00000429029.1:n.694-51T=
ENST00000523989.1:n.1805T=
NM_152419.2:c.1543-51T=	NP_689632.2:n.1543-51T=
XM_005273409.1:c.1654-51T=	XP_005273466.1:n.1654-51T=
XM_005273410.1:c.1630-51T=	XP_005273467.1:n.1630-51T=
XM_005273411.1:c.1462-51T=	XP_005273468.1:n.1462-51T=
NM_001363227.1:c.1630-51T=	NP_001350156.1:n.1630-51T=
NM_001363228.1:c.1351-51T=	NP_001350157.1:n.1351-51T=
NM_001363229.1:c.679-51T=	NP_001350158.1:n.679-51T=
NM_152419.3:c.1543-51T= MANE Select	NP_689632.2:n.1543-51T=
NM_001363227.2:c.1630-51T=	NP_001350156.1:n.1630-51T=
NM_001363228.2:c.1351-51T=	NP_001350157.1:n.1351-51T=
NM_001363229.2:c.679-51T=	NP_001350158.1:n.679-51T=