Canonical Allele Identifier: CA2687155747

Gene: HGSNAT

Linked Data

• gnomAD v4: 8-43199343-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43199343C>A , CM000670.2:g.43199343C>A	GRCh38
NC_000008.10:g.43054486C>A , CM000670.1:g.43054486C>A	GRCh37
NC_000008.9:g.43173643C>A	NCBI36
NG_009552.1:g.63895C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379644.9:c.1727-45C>A MANE Select	ENSP00000368965.4:n.1727-45C>A
ENST00000379644.8:c.1727-45C>A	ENSP00000368965.4:n.1727-45C>A
ENST00000519705.1:n.1043-45C>A
ENST00000521576.1:c.878-45C>A	ENSP00000429029.1:n.878-45C>A
NM_152419.2:c.1727-45C>A	NP_689632.2:n.1727-45C>A
XM_005273409.1:c.1838-45C>A	XP_005273466.1:n.1838-45C>A
XM_005273410.1:c.1814-45C>A	XP_005273467.1:n.1814-45C>A
XM_005273411.1:c.1646-45C>A	XP_005273468.1:n.1646-45C>A
NM_001363227.1:c.1814-45C>A	NP_001350156.1:n.1814-45C>A
NM_001363228.1:c.1535-45C>A	NP_001350157.1:n.1535-45C>A
NM_001363229.1:c.863-45C>A	NP_001350158.1:n.863-45C>A
NM_152419.3:c.1727-45C>A MANE Select	NP_689632.2:n.1727-45C>A
NM_001363227.2:c.1814-45C>A	NP_001350156.1:n.1814-45C>A
NM_001363228.2:c.1535-45C>A	NP_001350157.1:n.1535-45C>A
NM_001363229.2:c.863-45C>A	NP_001350158.1:n.863-45C>A