Canonical Allele Identifier: CA1779777456

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43199349T= , CM000670.2:g.43199349T=	GRCh38
NC_000008.10:g.43054492T= , CM000670.1:g.43054492T=	GRCh37
NC_000008.9:g.43173649T=	NCBI36
NG_009552.1:g.63901T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.1727-39T= MANE Select	ENSP00000368965.4:n.1727-39T=
ENST00000379644.8:c.1727-39T=	ENSP00000368965.4:n.1727-39T=
ENST00000519705.1:n.1043-39T=
ENST00000521576.1:c.878-39T=	ENSP00000429029.1:n.878-39T=
NM_152419.2:c.1727-39T=	NP_689632.2:n.1727-39T=
XM_005273409.1:c.1838-39T=	XP_005273466.1:n.1838-39T=
XM_005273410.1:c.1814-39T=	XP_005273467.1:n.1814-39T=
XM_005273411.1:c.1646-39T=	XP_005273468.1:n.1646-39T=
NM_001363227.1:c.1814-39T=	NP_001350156.1:n.1814-39T=
NM_001363228.1:c.1535-39T=	NP_001350157.1:n.1535-39T=
NM_001363229.1:c.863-39T=	NP_001350158.1:n.863-39T=
NM_152419.3:c.1727-39T= MANE Select	NP_689632.2:n.1727-39T=
NM_001363227.2:c.1814-39T=	NP_001350156.1:n.1814-39T=
NM_001363228.2:c.1535-39T=	NP_001350157.1:n.1535-39T=
NM_001363229.2:c.863-39T=	NP_001350158.1:n.863-39T=