Canonical Allele Identifier: CA371117323

Gene: HGSNAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43178191C>A , CM000670.2:g.43178191C>A	GRCh38
NC_000008.10:g.43033334C>A , CM000670.1:g.43033334C>A	GRCh37
NC_000008.9:g.43152491C>A	NCBI36
NG_009552.1:g.42743C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_152419.3:c.969C>A MANE Select	NP_689632.2:p.Cys323Ter
ENST00000379644.9:c.969C>A MANE Select	ENSP00000368965.4:p.Cys323Ter
NM_001363227.1:c.969C>A	NP_001350156.1:p.Cys323Ter
NM_001363227.2:c.969C>A	NP_001350156.1:p.Cys323Ter
NM_001363228.1:c.821-3954C>A	NP_001350157.1:n.821-3954C>A
NM_001363228.2:c.821-3954C>A	NP_001350157.1:n.821-3954C>A
NM_001363229.1:c.105C>A	NP_001350158.1:p.Cys35Ter
NM_001363229.2:c.105C>A	NP_001350158.1:p.Cys35Ter
NM_152419.2:c.969C>A	NP_689632.2:p.Cys323Ter
ENST00000379644.8:c.969C>A	ENSP00000368965.4:p.Cys323Ter
ENST00000522082.5:c.210C>A	ENSP00000430151.1:p.Cys70Ter
ENST00000524016.5:c.73C>A
XM_005273409.1:c.969C>A	XP_005273466.1:p.Cys323Ter
XM_005273410.1:c.969C>A	XP_005273467.1:p.Cys323Ter
XM_005273411.1:c.821-3954C>A	XP_005273468.1:n.821-3954C>A
XM_005273412.2:c.969C>A	XP_005273469.1:p.Cys323Ter
XM_005273412.4:c.969C>A	XP_005273469.1:p.Cys323Ter