Canonical Allele Identifier: CA397076590
Gene: GALNS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88835311T>G , CM000678.2:g.88835311T>G GRCh38
NC_000016.9:g.88901719T>G , CM000678.1:g.88901719T>G GRCh37
NC_000016.8:g.87429220T>G NCBI36
NG_008667.1:g.26656A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.800A>C MANE Select ENSP00000268695.5:p.Lys267Thr
ENST00000268695.9:c.800A>C ENSP00000268695.5:p.Lys267Thr
ENST00000562593.5:n.4209A>C
ENST00000562931.5:n.388A>C
ENST00000567525.5:c.481A>C ENSP00000454484.1:n.481A>C
ENST00000568613.5:c.919A>C ENSP00000457921.1:n.919A>C
NM_000512.4:c.800A>C NP_000503.1:p.Lys267Thr
XM_005256301.2:c.800A>C XP_005256358.1:p.Lys267Thr
XM_005256302.1:c.818A>C XP_005256359.1:p.Lys273Thr
XM_011522982.1:c.818A>C XP_011521284.1:p.Lys273Thr
XM_011522984.1:c.818A>C XP_011521286.1:p.Lys273Thr
NM_001323543.1:c.245A>C NP_001310472.1:p.Lys82Thr
NM_001323544.1:c.818A>C NP_001310473.1:p.Lys273Thr
XM_005256301.3:c.800A>C XP_005256358.1:p.Lys267Thr
XM_011522982.2:c.818A>C XP_011521284.1:p.Lys273Thr
XM_017023111.2:c.818A>C XP_016878600.1:p.Lys273Thr
XM_017023112.2:c.818A>C XP_016878601.1:p.Lys273Thr
XM_017023113.1:c.245A>C XP_016878602.1:p.Lys82Thr
NM_000512.5:c.800A>C MANE Select NP_000503.1:p.Lys267Thr
NM_001323543.2:c.245A>C NP_001310472.1:p.Lys82Thr
NM_001323544.2:c.818A>C NP_001310473.1:p.Lys273Thr