Canonical Allele Identifier: CA1779762425

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43197633T= , CM000670.2:g.43197633T=	GRCh38
NC_000008.10:g.43052776T= , CM000670.1:g.43052776T=	GRCh37
NC_000008.9:g.43171933T=	NCBI36
NG_009552.1:g.62185T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379644.9:c.1543-39T= MANE Select	ENSP00000368965.4:n.1543-39T=
ENST00000379644.8:c.1543-39T=	ENSP00000368965.4:n.1543-39T=
ENST00000519705.1:n.859-39T=
ENST00000521576.1:c.694-39T=	ENSP00000429029.1:n.694-39T=
ENST00000523989.1:n.1817T=
NM_152419.2:c.1543-39T=	NP_689632.2:n.1543-39T=
XM_005273409.1:c.1654-39T=	XP_005273466.1:n.1654-39T=
XM_005273410.1:c.1630-39T=	XP_005273467.1:n.1630-39T=
XM_005273411.1:c.1462-39T=	XP_005273468.1:n.1462-39T=
NM_001363227.1:c.1630-39T=	NP_001350156.1:n.1630-39T=
NM_001363228.1:c.1351-39T=	NP_001350157.1:n.1351-39T=
NM_001363229.1:c.679-39T=	NP_001350158.1:n.679-39T=
NM_152419.3:c.1543-39T= MANE Select	NP_689632.2:n.1543-39T=
NM_001363227.2:c.1630-39T=	NP_001350156.1:n.1630-39T=
NM_001363228.2:c.1351-39T=	NP_001350157.1:n.1351-39T=
NM_001363229.2:c.679-39T=	NP_001350158.1:n.679-39T=