Canonical Allele Identifier: CA980349249
Gene: GALNS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88835977_88835978del , CM000678.2:g.88835977_88835978del GRCh38
NC_000016.9:g.88902385_88902386del , CM000678.1:g.88902385_88902386del GRCh37
NC_000016.8:g.87429886_87429887del NCBI36
NG_008667.1:g.25989_25990del

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.634-129_634-128del MANE Select ENSP00000268695.5:n.634-129_634-128del
ENST00000268695.9:c.634-129_634-128del ENSP00000268695.5:n.634-129_634-128del
ENST00000562593.5:n.4043-129_4043-128del
ENST00000562831.1:c.418-129_418-128del ENSP00000455174.1:n.418-129_418-128del
ENST00000562931.5:n.222-129_222-128del
ENST00000566563.1:n.336-129_336-128del
ENST00000567525.5:c.315-129_315-128del ENSP00000454484.1:n.315-129_315-128del
ENST00000568613.5:c.753-129_753-128del ENSP00000457921.1:n.753-129_753-128del
NM_000512.4:c.634-129_634-128del NP_000503.1:n.634-129_634-128del
XM_005256301.2:c.634-129_634-128del XP_005256358.1:n.634-129_634-128del
XM_005256302.1:c.652-129_652-128del XP_005256359.1:n.652-129_652-128del
XM_011522982.1:c.652-129_652-128del XP_011521284.1:n.652-129_652-128del
XM_011522984.1:c.652-129_652-128del XP_011521286.1:n.652-129_652-128del
NM_001323543.1:c.79-129_79-128del NP_001310472.1:n.79-129_79-128del
NM_001323544.1:c.652-129_652-128del NP_001310473.1:n.652-129_652-128del
XM_005256301.3:c.634-129_634-128del XP_005256358.1:n.634-129_634-128del
XM_011522982.2:c.652-129_652-128del XP_011521284.1:n.652-129_652-128del
XM_017023111.2:c.652-129_652-128del XP_016878600.1:n.652-129_652-128del
XM_017023112.2:c.652-129_652-128del XP_016878601.1:n.652-129_652-128del
XM_017023113.1:c.79-129_79-128del XP_016878602.1:n.79-129_79-128del
NM_000512.5:c.634-129_634-128del MANE Select NP_000503.1:n.634-129_634-128del
NM_001323543.2:c.79-129_79-128del NP_001310472.1:n.79-129_79-128del
NM_001323544.2:c.652-129_652-128del NP_001310473.1:n.652-129_652-128del