Canonical Allele Identifier: CA397076595
Gene: GALNS HGNC NCBI

Linked Data

dbSNP Id: rs1196349459

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88835312T>C , CM000678.2:g.88835312T>C GRCh38
NC_000016.9:g.88901720T>C , CM000678.1:g.88901720T>C GRCh37
NC_000016.8:g.87429221T>C NCBI36
NG_008667.1:g.26655A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.799A>G MANE Select ENSP00000268695.5:p.Lys267Glu
ENST00000268695.9:c.799A>G ENSP00000268695.5:p.Lys267Glu
ENST00000562593.5:n.4208A>G
ENST00000562931.5:n.387A>G
ENST00000567525.5:c.480A>G ENSP00000454484.1:n.480A>G
ENST00000568613.5:c.918A>G ENSP00000457921.1:n.918A>G
NM_000512.4:c.799A>G NP_000503.1:p.Lys267Glu
XM_005256301.2:c.799A>G XP_005256358.1:p.Lys267Glu
XM_005256302.1:c.817A>G XP_005256359.1:p.Lys273Glu
XM_011522982.1:c.817A>G XP_011521284.1:p.Lys273Glu
XM_011522984.1:c.817A>G XP_011521286.1:p.Lys273Glu
NM_001323543.1:c.244A>G NP_001310472.1:p.Lys82Glu
NM_001323544.1:c.817A>G NP_001310473.1:p.Lys273Glu
XM_005256301.3:c.799A>G XP_005256358.1:p.Lys267Glu
XM_011522982.2:c.817A>G XP_011521284.1:p.Lys273Glu
XM_017023111.2:c.817A>G XP_016878600.1:p.Lys273Glu
XM_017023112.2:c.817A>G XP_016878601.1:p.Lys273Glu
XM_017023113.1:c.244A>G XP_016878602.1:p.Lys82Glu
NM_000512.5:c.799A>G MANE Select NP_000503.1:p.Lys267Glu
NM_001323543.2:c.244A>G NP_001310472.1:p.Lys82Glu
NM_001323544.2:c.817A>G NP_001310473.1:p.Lys273Glu