Canonical Allele Identifier: CA397101217
Community Standard Title: NM_000512.5(GALNS):c.949G>C (p.Gly317Arg)
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88832051C>G , CM000678.2:g.88832051C>G GRCh38
NC_000016.9:g.88898459C>G , CM000678.1:g.88898459C>G GRCh37
NC_000016.8:g.87425960C>G NCBI36
NG_008667.1:g.29916G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000512.5:c.949G>C MANE Select NP_000503.1:p.Gly317Arg
ENST00000268695.10:c.949G>C MANE Select ENSP00000268695.5:p.Gly317Arg
NM_000512.4:c.949G>C NP_000503.1:p.Gly317Arg
NM_001323543.1:c.394G>C NP_001310472.1:p.Gly132Arg
NM_001323543.2:c.394G>C NP_001310472.1:p.Gly132Arg
NM_001323544.1:c.967G>C NP_001310473.1:p.Gly323Arg
NM_001323544.2:c.967G>C NP_001310473.1:p.Gly323Arg
ENST00000268695.9:c.949G>C ENSP00000268695.5:p.Gly317Arg
ENST00000562593.5:n.4358G>C
ENST00000562931.5:n.537G>C
ENST00000567525.5:c.630G>C ENSP00000454484.1:n.630G>C
ENST00000568613.5:c.1068G>C ENSP00000457921.1:n.1068G>C
XM_005256301.2:c.949G>C XP_005256358.1:p.Gly317Arg
XM_005256301.3:c.949G>C XP_005256358.1:p.Gly317Arg
XM_005256302.1:c.967G>C XP_005256359.1:p.Gly323Arg
XM_011522982.1:c.967G>C XP_011521284.1:p.Gly323Arg
XM_011522982.2:c.967G>C XP_011521284.1:p.Gly323Arg
XM_011522984.1:c.967G>C XP_011521286.1:p.Gly323Arg
XM_017023111.2:c.967G>C XP_016878600.1:p.Gly323Arg
XM_017023112.2:c.967G>C XP_016878601.1:p.Gly323Arg
XM_017023113.1:c.394G>C XP_016878602.1:p.Gly132Arg