Canonical Allele Identifier: CA2241317358
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88824848G= , CM000678.2:g.88824848G= GRCh38
NC_000016.9:g.88891256G= , CM000678.1:g.88891256G= GRCh37
NC_000016.8:g.87418757G= NCBI36
NG_008667.1:g.37119C=

Transcript Alleles

HGVS Amino-acid change
ENST00000268695.10:c.1161C= MANE Select ENSP00000268695.5:p.Gly387=
ENST00000268695.9:c.1161C= ENSP00000268695.5:p.Gly387=
ENST00000562593.5:n.4570C=
ENST00000564263.1:n.437C=
ENST00000567525.5:c.842C= ENSP00000454484.1:n.842C=
ENST00000568613.5:c.1280C= ENSP00000457921.1:n.1280C=
NM_000512.4:c.1161C= NP_000503.1:p.Gly387=
XM_005256301.2:c.1161C= XP_005256358.1:p.Gly387=
XM_005256302.1:c.1179C= XP_005256359.1:p.Gly393=
XM_011522982.1:c.1179C= XP_011521284.1:p.Gly393=
XM_011522984.1:c.1179C= XP_011521286.1:p.Gly393=
NM_001323543.1:c.606C= NP_001310472.1:p.Gly202=
NM_001323544.1:c.1179C= NP_001310473.1:p.Gly393=
XM_005256301.3:c.1161C= XP_005256358.1:p.Gly387=
XM_011522982.2:c.1179C= XP_011521284.1:p.Gly393=
XM_017023111.2:c.1179C= XP_016878600.1:p.Gly393=
XM_017023112.2:c.1179C= XP_016878601.1:p.Gly393=
XM_017023113.1:c.606C= XP_016878602.1:p.Gly202=
NM_000512.5:c.1161C= MANE Select NP_000503.1:p.Gly387=
NM_001323543.2:c.606C= NP_001310472.1:p.Gly202=
NM_001323544.2:c.1179C= NP_001310473.1:p.Gly393=