Canonical Allele Identifier: CA2634895260
Gene: GALNS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88840854_88840896del , CM000678.2:g.88840854_88840896del GRCh38
NC_000016.9:g.88907262_88907304del , CM000678.1:g.88907262_88907304del GRCh37
NC_000016.8:g.87434763_87434805del NCBI36
NG_008667.1:g.21078_21120del

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.422+103_422+145del MANE Select ENSP00000268695.5:n.422+103_422+145del
ENST00000268695.9:c.422+103_422+145del ENSP00000268695.5:n.422+103_422+145del
ENST00000562593.5:n.3831+103_3831+145del
ENST00000562831.1:c.206+103_206+145del ENSP00000455174.1:n.206+103_206+145del
ENST00000565364.1:n.558-37_563del
ENST00000567525.5:c.247+103_247+145del ENSP00000454484.1:n.247+103_247+145del
ENST00000567779.1:n.355_397del
ENST00000568613.5:c.541+103_541+145del ENSP00000457921.1:n.541+103_541+145del
NM_000512.4:c.422+103_422+145del NP_000503.1:n.422+103_422+145del
XM_005256301.2:c.422+103_422+145del XP_005256358.1:n.422+103_422+145del
XM_005256302.1:c.440+103_440+145del XP_005256359.1:n.440+103_440+145del
XM_011522982.1:c.440+103_440+145del XP_011521284.1:n.440+103_440+145del
XM_011522984.1:c.440+103_440+145del XP_011521286.1:n.440+103_440+145del
NM_001323543.1:c.-134+103_-134+145del NP_001310472.1:n.-134+103_-134+145del
NM_001323544.1:c.440+103_440+145del NP_001310473.1:n.440+103_440+145del
XM_005256301.3:c.422+103_422+145del XP_005256358.1:n.422+103_422+145del
XM_011522982.2:c.440+103_440+145del XP_011521284.1:n.440+103_440+145del
XM_017023111.2:c.440+103_440+145del XP_016878600.1:n.440+103_440+145del
XM_017023112.2:c.440+103_440+145del XP_016878601.1:n.440+103_440+145del
XM_017023113.1:c.-134+103_-134+145del XP_016878602.1:n.-134+103_-134+145del
NM_000512.5:c.422+103_422+145del MANE Select NP_000503.1:n.422+103_422+145del
NM_001323543.2:c.-134+103_-134+145del NP_001310472.1:n.-134+103_-134+145del
NM_001323544.2:c.440+103_440+145del NP_001310473.1:n.440+103_440+145del