Canonical Allele Identifier: CA397087590

Gene: GALNS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88840998C>T , CM000678.2:g.88840998C>T	GRCh38
NC_000016.9:g.88907406C>T , CM000678.1:g.88907406C>T	GRCh37
NC_000016.8:g.87434907C>T	NCBI36
NG_008667.1:g.20969G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000512.5:c.416G>A MANE Select	NP_000503.1:p.Gly139Asp
ENST00000268695.10:c.416G>A MANE Select	ENSP00000268695.5:p.Gly139Asp
NM_000512.4:c.416G>A	NP_000503.1:p.Gly139Asp
NM_001323543.1:c.-140G>A	NP_001310472.1:n.-140G>A
NM_001323543.2:c.-140G>A	NP_001310472.1:n.-140G>A
NM_001323544.1:c.434G>A	NP_001310473.1:p.Gly145Asp
NM_001323544.2:c.434G>A	NP_001310473.1:p.Gly145Asp
ENST00000268695.9:c.416G>A	ENSP00000268695.5:p.Gly139Asp
ENST00000562593.5:n.3825G>A
ENST00000562831.1:c.200G>A	ENSP00000455174.1:p.Gly67Asp
ENST00000565364.1:n.551G>A
ENST00000567525.5:c.241G>A	ENSP00000454484.1:n.241G>A
ENST00000567779.1:n.246G>A
ENST00000568613.5:c.535G>A	ENSP00000457921.1:n.535G>A
XM_005256301.2:c.416G>A	XP_005256358.1:p.Gly139Asp
XM_005256301.3:c.416G>A	XP_005256358.1:p.Gly139Asp
XM_005256302.1:c.434G>A	XP_005256359.1:p.Gly145Asp
XM_011522982.1:c.434G>A	XP_011521284.1:p.Gly145Asp
XM_011522982.2:c.434G>A	XP_011521284.1:p.Gly145Asp
XM_011522984.1:c.434G>A	XP_011521286.1:p.Gly145Asp
XM_017023111.2:c.434G>A	XP_016878600.1:p.Gly145Asp
XM_017023112.2:c.434G>A	XP_016878601.1:p.Gly145Asp
XM_017023113.1:c.-140G>A	XP_016878602.1:n.-140G>A