Canonical Allele Identifier: CA221055

Gene: GALNS

Linked Data

• ClinVar Variation Id: 93176
• ClinVar RCV Id: RCV000079034
• dbSNP Id: rs398123436
• MyVariant Identifiers: chr16:g.88908358C>A (hg19) ; chr16:g.88841950C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88841950C>A , CM000678.2:g.88841950C>A	GRCh38
NC_000016.9:g.88908358C>A , CM000678.1:g.88908358C>A	GRCh37
NC_000016.8:g.87435859C>A	NCBI36
NG_008667.1:g.20017G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000268695.10:c.266G>T MANE Select	ENSP00000268695.5:p.Gly89Val
ENST00000268695.9:c.266G>T	ENSP00000268695.5:p.Gly89Val
ENST00000562593.5:n.3675G>T
ENST00000562831.1:c.50G>T	ENSP00000455174.1:p.Gly17Val
ENST00000565364.1:n.401G>T
ENST00000567525.5:c.91G>T	ENSP00000454484.1:p.Asp31Tyr
ENST00000567779.1:n.96G>T
ENST00000568613.5:c.385G>T	ENSP00000457921.1:n.385G>T
NM_000512.4:c.266G>T	NP_000503.1:p.Gly89Val
XM_005256301.2:c.266G>T	XP_005256358.1:p.Gly89Val
XM_005256302.1:c.284G>T	XP_005256359.1:p.Gly95Val
XM_011522982.1:c.284G>T	XP_011521284.1:p.Gly95Val
XM_011522984.1:c.284G>T	XP_011521286.1:p.Gly95Val
NM_001323543.1:c.-290G>T	NP_001310472.1:n.-290G>T
NM_001323544.1:c.284G>T	NP_001310473.1:p.Gly95Val
XM_005256301.3:c.266G>T	XP_005256358.1:p.Gly89Val
XM_011522982.2:c.284G>T	XP_011521284.1:p.Gly95Val
XM_017023111.2:c.284G>T	XP_016878600.1:p.Gly95Val
XM_017023112.2:c.284G>T	XP_016878601.1:p.Gly95Val
XM_017023113.1:c.-290G>T	XP_016878602.1:n.-290G>T
NM_000512.5:c.266G>T MANE Select	NP_000503.1:p.Gly89Val
NM_001323543.2:c.-290G>T	NP_001310472.1:n.-290G>T
NM_001323544.2:c.284G>T	NP_001310473.1:p.Gly95Val