Canonical Allele Identifier: CA980343511
Gene: GALNS HGNC NCBI

Linked Data

dbSNP Id: rs1910902474

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88826304_88826352del , CM000678.2:g.88826304_88826352del GRCh38
NC_000016.9:g.88892712_88892760del , CM000678.1:g.88892712_88892760del GRCh37
NC_000016.8:g.87420213_87420261del NCBI36
NG_008667.1:g.35627_35675del

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.1139+362_1139+410del MANE Select ENSP00000268695.5:n.1139+362_1139+410del
ENST00000268695.9:c.1139+362_1139+410del ENSP00000268695.5:n.1139+362_1139+410del
ENST00000562593.5:n.4548+362_4548+410del
ENST00000564263.1:n.415+362_415+410del
ENST00000567525.5:c.820+362_820+410del ENSP00000454484.1:n.820+362_820+410del
ENST00000568613.5:c.1258+362_1258+410del ENSP00000457921.1:n.1258+362_1258+410del
NM_000512.4:c.1139+362_1139+410del NP_000503.1:n.1139+362_1139+410del
XM_005256301.2:c.1139+362_1139+410del XP_005256358.1:n.1139+362_1139+410del
XM_005256302.1:c.1157+362_1157+410del XP_005256359.1:n.1157+362_1157+410del
XM_011522982.1:c.1157+362_1157+410del XP_011521284.1:n.1157+362_1157+410del
XM_011522984.1:c.1157+362_1157+410del XP_011521286.1:n.1157+362_1157+410del
NM_001323543.1:c.584+362_584+410del NP_001310472.1:n.584+362_584+410del
NM_001323544.1:c.1157+362_1157+410del NP_001310473.1:n.1157+362_1157+410del
XM_005256301.3:c.1139+362_1139+410del XP_005256358.1:n.1139+362_1139+410del
XM_011522982.2:c.1157+362_1157+410del XP_011521284.1:n.1157+362_1157+410del
XM_017023111.2:c.1157+362_1157+410del XP_016878600.1:n.1157+362_1157+410del
XM_017023112.2:c.1157+362_1157+410del XP_016878601.1:n.1157+362_1157+410del
XM_017023113.1:c.584+362_584+410del XP_016878602.1:n.584+362_584+410del
NM_000512.5:c.1139+362_1139+410del MANE Select NP_000503.1:n.1139+362_1139+410del
NM_001323543.2:c.584+362_584+410del NP_001310472.1:n.584+362_584+410del
NM_001323544.2:c.1157+362_1157+410del NP_001310473.1:n.1157+362_1157+410del