Canonical Allele Identifier: CA2241326039
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88837704A= , CM000678.2:g.88837704A= GRCh38
NC_000016.9:g.88904112A= , CM000678.1:g.88904112A= GRCh37
NC_000016.8:g.87431613A= NCBI36
NG_008667.1:g.24263T=

Transcript Alleles

HGVS Amino-acid change
ENST00000268695.10:c.484T= MANE Select ENSP00000268695.5:p.Ser162=
ENST00000268695.9:c.484T= ENSP00000268695.5:p.Ser162=
ENST00000561812.1:n.440T=
ENST00000562593.5:n.3893T=
ENST00000562831.1:c.268T= ENSP00000455174.1:p.Ser90=
ENST00000562931.5:n.72T=
ENST00000566563.1:n.186T=
ENST00000567525.5:c.248-1437T= ENSP00000454484.1:n.248-1437T=
ENST00000568613.5:c.603T= ENSP00000457921.1:n.603T=
NM_000512.4:c.484T= NP_000503.1:p.Ser162=
XM_005256301.2:c.484T= XP_005256358.1:p.Ser162=
XM_005256302.1:c.502T= XP_005256359.1:p.Ser168=
XM_011522982.1:c.502T= XP_011521284.1:p.Ser168=
XM_011522984.1:c.502T= XP_011521286.1:p.Ser168=
NM_001323543.1:c.-72T= NP_001310472.1:n.-72T=
NM_001323544.1:c.502T= NP_001310473.1:p.Ser168=
XM_005256301.3:c.484T= XP_005256358.1:p.Ser162=
XM_011522982.2:c.502T= XP_011521284.1:p.Ser168=
XM_017023111.2:c.502T= XP_016878600.1:p.Ser168=
XM_017023112.2:c.502T= XP_016878601.1:p.Ser168=
XM_017023113.1:c.-72T= XP_016878602.1:n.-72T=
NM_000512.5:c.484T= MANE Select NP_000503.1:p.Ser162=
NM_001323543.2:c.-72T= NP_001310472.1:n.-72T=
NM_001323544.2:c.502T= NP_001310473.1:p.Ser168=