Canonical Allele Identifier: CA980343573
Gene: GALNS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88826331_88826428del , CM000678.2:g.88826331_88826428del GRCh38
NC_000016.9:g.88892739_88892836del , CM000678.1:g.88892739_88892836del GRCh37
NC_000016.8:g.87420240_87420337del NCBI36
NG_008667.1:g.35554_35651del

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.1139+289_1139+386del MANE Select ENSP00000268695.5:n.1139+289_1139+386del
ENST00000268695.9:c.1139+289_1139+386del ENSP00000268695.5:n.1139+289_1139+386del
ENST00000562593.5:n.4548+289_4548+386del
ENST00000564263.1:n.415+289_415+386del
ENST00000567525.5:c.820+289_820+386del ENSP00000454484.1:n.820+289_820+386del
ENST00000568613.5:c.1258+289_1258+386del ENSP00000457921.1:n.1258+289_1258+386del
NM_000512.4:c.1139+289_1139+386del NP_000503.1:n.1139+289_1139+386del
XM_005256301.2:c.1139+289_1139+386del XP_005256358.1:n.1139+289_1139+386del
XM_005256302.1:c.1157+289_1157+386del XP_005256359.1:n.1157+289_1157+386del
XM_011522982.1:c.1157+289_1157+386del XP_011521284.1:n.1157+289_1157+386del
XM_011522984.1:c.1157+289_1157+386del XP_011521286.1:n.1157+289_1157+386del
NM_001323543.1:c.584+289_584+386del NP_001310472.1:n.584+289_584+386del
NM_001323544.1:c.1157+289_1157+386del NP_001310473.1:n.1157+289_1157+386del
XM_005256301.3:c.1139+289_1139+386del XP_005256358.1:n.1139+289_1139+386del
XM_011522982.2:c.1157+289_1157+386del XP_011521284.1:n.1157+289_1157+386del
XM_017023111.2:c.1157+289_1157+386del XP_016878600.1:n.1157+289_1157+386del
XM_017023112.2:c.1157+289_1157+386del XP_016878601.1:n.1157+289_1157+386del
XM_017023113.1:c.584+289_584+386del XP_016878602.1:n.584+289_584+386del
NM_000512.5:c.1139+289_1139+386del MANE Select NP_000503.1:n.1139+289_1139+386del
NM_001323543.2:c.584+289_584+386del NP_001310472.1:n.584+289_584+386del
NM_001323544.2:c.1157+289_1157+386del NP_001310473.1:n.1157+289_1157+386del