Canonical Allele Identifier: CA980343567
Gene: GALNS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88826313_88826410del , CM000678.2:g.88826313_88826410del GRCh38
NC_000016.9:g.88892721_88892818del , CM000678.1:g.88892721_88892818del GRCh37
NC_000016.8:g.87420222_87420319del NCBI36
NG_008667.1:g.35561_35658del

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.1139+296_1139+393del MANE Select ENSP00000268695.5:n.1139+296_1139+393del
ENST00000268695.9:c.1139+296_1139+393del ENSP00000268695.5:n.1139+296_1139+393del
ENST00000562593.5:n.4548+296_4548+393del
ENST00000564263.1:n.415+296_415+393del
ENST00000567525.5:c.820+296_820+393del ENSP00000454484.1:n.820+296_820+393del
ENST00000568613.5:c.1258+296_1258+393del ENSP00000457921.1:n.1258+296_1258+393del
NM_000512.4:c.1139+296_1139+393del NP_000503.1:n.1139+296_1139+393del
XM_005256301.2:c.1139+296_1139+393del XP_005256358.1:n.1139+296_1139+393del
XM_005256302.1:c.1157+296_1157+393del XP_005256359.1:n.1157+296_1157+393del
XM_011522982.1:c.1157+296_1157+393del XP_011521284.1:n.1157+296_1157+393del
XM_011522984.1:c.1157+296_1157+393del XP_011521286.1:n.1157+296_1157+393del
NM_001323543.1:c.584+296_584+393del NP_001310472.1:n.584+296_584+393del
NM_001323544.1:c.1157+296_1157+393del NP_001310473.1:n.1157+296_1157+393del
XM_005256301.3:c.1139+296_1139+393del XP_005256358.1:n.1139+296_1139+393del
XM_011522982.2:c.1157+296_1157+393del XP_011521284.1:n.1157+296_1157+393del
XM_017023111.2:c.1157+296_1157+393del XP_016878600.1:n.1157+296_1157+393del
XM_017023112.2:c.1157+296_1157+393del XP_016878601.1:n.1157+296_1157+393del
XM_017023113.1:c.584+296_584+393del XP_016878602.1:n.584+296_584+393del
NM_000512.5:c.1139+296_1139+393del MANE Select NP_000503.1:n.1139+296_1139+393del
NM_001323543.2:c.584+296_584+393del NP_001310472.1:n.584+296_584+393del
NM_001323544.2:c.1157+296_1157+393del NP_001310473.1:n.1157+296_1157+393del