Canonical Allele Identifier: CA980349196
Gene: GALNS HGNC NCBI

Linked Data

dbSNP Id: rs1567531499

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88835979_88836018dup , CM000678.2:g.88835979_88836018dup GRCh38
NC_000016.9:g.88902387_88902426dup , CM000678.1:g.88902387_88902426dup GRCh37
NC_000016.8:g.87429888_87429927dup NCBI36
NG_008667.1:g.25988_26027dup

Transcript Alleles

HGVS Amino-acid change
ENST00000268695.10:c.634-130_634-91dup MANE Select ENSP00000268695.5:n.634-130_634-91dup
ENST00000268695.9:c.634-130_634-91dup ENSP00000268695.5:n.634-130_634-91dup
ENST00000562593.5:n.4043-130_4043-91dup
ENST00000562831.1:c.418-130_418-91dup ENSP00000455174.1:n.418-130_418-91dup
ENST00000562931.5:n.222-130_222-91dup
ENST00000566563.1:n.336-130_336-91dup
ENST00000567525.5:c.315-130_315-91dup ENSP00000454484.1:n.315-130_315-91dup
ENST00000568613.5:c.753-130_753-91dup ENSP00000457921.1:n.753-130_753-91dup
NM_000512.4:c.634-130_634-91dup NP_000503.1:n.634-130_634-91dup
XM_005256301.2:c.634-130_634-91dup XP_005256358.1:n.634-130_634-91dup
XM_005256302.1:c.652-130_652-91dup XP_005256359.1:n.652-130_652-91dup
XM_011522982.1:c.652-130_652-91dup XP_011521284.1:n.652-130_652-91dup
XM_011522984.1:c.652-130_652-91dup XP_011521286.1:n.652-130_652-91dup
NM_001323543.1:c.79-130_79-91dup NP_001310472.1:n.79-130_79-91dup
NM_001323544.1:c.652-130_652-91dup NP_001310473.1:n.652-130_652-91dup
XM_005256301.3:c.634-130_634-91dup XP_005256358.1:n.634-130_634-91dup
XM_011522982.2:c.652-130_652-91dup XP_011521284.1:n.652-130_652-91dup
XM_017023111.2:c.652-130_652-91dup XP_016878600.1:n.652-130_652-91dup
XM_017023112.2:c.652-130_652-91dup XP_016878601.1:n.652-130_652-91dup
XM_017023113.1:c.79-130_79-91dup XP_016878602.1:n.79-130_79-91dup
NM_000512.5:c.634-130_634-91dup MANE Select NP_000503.1:n.634-130_634-91dup
NM_001323543.2:c.79-130_79-91dup NP_001310472.1:n.79-130_79-91dup
NM_001323544.2:c.652-130_652-91dup NP_001310473.1:n.652-130_652-91dup