Canonical Allele Identifier: CA980343468
Gene: GALNS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88826297_88826394del , CM000678.2:g.88826297_88826394del GRCh38
NC_000016.9:g.88892705_88892802del , CM000678.1:g.88892705_88892802del GRCh37
NC_000016.8:g.87420206_87420303del NCBI36
NG_008667.1:g.35598_35695del

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.1139+333_1139+430del MANE Select ENSP00000268695.5:n.1139+333_1139+430del
ENST00000268695.9:c.1139+333_1139+430del ENSP00000268695.5:n.1139+333_1139+430del
ENST00000562593.5:n.4548+333_4548+430del
ENST00000564263.1:n.415+333_415+430del
ENST00000567525.5:c.820+333_820+430del ENSP00000454484.1:n.820+333_820+430del
ENST00000568613.5:c.1258+333_1258+430del ENSP00000457921.1:n.1258+333_1258+430del
NM_000512.4:c.1139+333_1139+430del NP_000503.1:n.1139+333_1139+430del
XM_005256301.2:c.1139+333_1139+430del XP_005256358.1:n.1139+333_1139+430del
XM_005256302.1:c.1157+333_1157+430del XP_005256359.1:n.1157+333_1157+430del
XM_011522982.1:c.1157+333_1157+430del XP_011521284.1:n.1157+333_1157+430del
XM_011522984.1:c.1157+333_1157+430del XP_011521286.1:n.1157+333_1157+430del
NM_001323543.1:c.584+333_584+430del NP_001310472.1:n.584+333_584+430del
NM_001323544.1:c.1157+333_1157+430del NP_001310473.1:n.1157+333_1157+430del
XM_005256301.3:c.1139+333_1139+430del XP_005256358.1:n.1139+333_1139+430del
XM_011522982.2:c.1157+333_1157+430del XP_011521284.1:n.1157+333_1157+430del
XM_017023111.2:c.1157+333_1157+430del XP_016878600.1:n.1157+333_1157+430del
XM_017023112.2:c.1157+333_1157+430del XP_016878601.1:n.1157+333_1157+430del
XM_017023113.1:c.584+333_584+430del XP_016878602.1:n.584+333_584+430del
NM_000512.5:c.1139+333_1139+430del MANE Select NP_000503.1:n.1139+333_1139+430del
NM_001323543.2:c.584+333_584+430del NP_001310472.1:n.584+333_584+430del
NM_001323544.2:c.1157+333_1157+430del NP_001310473.1:n.1157+333_1157+430del