Canonical Allele Identifier: CA397087888
Gene: GALNS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88841029T>G , CM000678.2:g.88841029T>G GRCh38
NC_000016.9:g.88907437T>G , CM000678.1:g.88907437T>G GRCh37
NC_000016.8:g.87434938T>G NCBI36
NG_008667.1:g.20938A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.385A>C MANE Select ENSP00000268695.5:p.Lys129Gln
ENST00000268695.9:c.385A>C ENSP00000268695.5:p.Lys129Gln
ENST00000562593.5:n.3794A>C
ENST00000562831.1:c.169A>C ENSP00000455174.1:p.Lys57Gln
ENST00000565364.1:n.520A>C
ENST00000567525.5:c.210A>C ENSP00000454484.1:p.Ter70Cys
ENST00000567779.1:n.215A>C
ENST00000568613.5:c.504A>C ENSP00000457921.1:n.504A>C
NM_000512.4:c.385A>C NP_000503.1:p.Lys129Gln
XM_005256301.2:c.385A>C XP_005256358.1:p.Lys129Gln
XM_005256302.1:c.403A>C XP_005256359.1:p.Lys135Gln
XM_011522982.1:c.403A>C XP_011521284.1:p.Lys135Gln
XM_011522984.1:c.403A>C XP_011521286.1:p.Lys135Gln
NM_001323543.1:c.-171A>C NP_001310472.1:n.-171A>C
NM_001323544.1:c.403A>C NP_001310473.1:p.Lys135Gln
XM_005256301.3:c.385A>C XP_005256358.1:p.Lys129Gln
XM_011522982.2:c.403A>C XP_011521284.1:p.Lys135Gln
XM_017023111.2:c.403A>C XP_016878600.1:p.Lys135Gln
XM_017023112.2:c.403A>C XP_016878601.1:p.Lys135Gln
XM_017023113.1:c.-171A>C XP_016878602.1:n.-171A>C
NM_000512.5:c.385A>C MANE Select NP_000503.1:p.Lys129Gln
NM_001323543.2:c.-171A>C NP_001310472.1:n.-171A>C
NM_001323544.2:c.403A>C NP_001310473.1:p.Lys135Gln