Canonical Allele Identifier: CA397083366
Gene: GALNS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88837725C>G , CM000678.2:g.88837725C>G GRCh38
NC_000016.9:g.88904133C>G , CM000678.1:g.88904133C>G GRCh37
NC_000016.8:g.87431634C>G NCBI36
NG_008667.1:g.24242G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.463G>C MANE Select ENSP00000268695.5:p.Gly155Arg
ENST00000268695.9:c.463G>C ENSP00000268695.5:p.Gly155Arg
ENST00000561812.1:n.419G>C
ENST00000562593.5:n.3872G>C
ENST00000562831.1:c.247G>C ENSP00000455174.1:p.Gly83Arg
ENST00000562931.5:n.51G>C
ENST00000566563.1:n.165G>C
ENST00000567525.5:c.248-1458G>C ENSP00000454484.1:n.248-1458G>C
ENST00000568613.5:c.582G>C ENSP00000457921.1:n.582G>C
NM_000512.4:c.463G>C NP_000503.1:p.Gly155Arg
XM_005256301.2:c.463G>C XP_005256358.1:p.Gly155Arg
XM_005256302.1:c.481G>C XP_005256359.1:p.Gly161Arg
XM_011522982.1:c.481G>C XP_011521284.1:p.Gly161Arg
XM_011522984.1:c.481G>C XP_011521286.1:p.Gly161Arg
NM_001323543.1:c.-93G>C NP_001310472.1:n.-93G>C
NM_001323544.1:c.481G>C NP_001310473.1:p.Gly161Arg
XM_005256301.3:c.463G>C XP_005256358.1:p.Gly155Arg
XM_011522982.2:c.481G>C XP_011521284.1:p.Gly161Arg
XM_017023111.2:c.481G>C XP_016878600.1:p.Gly161Arg
XM_017023112.2:c.481G>C XP_016878601.1:p.Gly161Arg
XM_017023113.1:c.-93G>C XP_016878602.1:n.-93G>C
NM_000512.5:c.463G>C MANE Select NP_000503.1:p.Gly155Arg
NM_001323543.2:c.-93G>C NP_001310472.1:n.-93G>C
NM_001323544.2:c.481G>C NP_001310473.1:p.Gly161Arg