Canonical Allele Identifier: CA2241326038
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88837703G= , CM000678.2:g.88837703G= GRCh38
NC_000016.9:g.88904111G= , CM000678.1:g.88904111G= GRCh37
NC_000016.8:g.87431612G= NCBI36
NG_008667.1:g.24264C=

Transcript Alleles

HGVS Amino-acid change
ENST00000268695.10:c.485C= MANE Select ENSP00000268695.5:p.Ser162=
ENST00000268695.9:c.485C= ENSP00000268695.5:p.Ser162=
ENST00000561812.1:n.441C=
ENST00000562593.5:n.3894C=
ENST00000562831.1:c.269C= ENSP00000455174.1:p.Ser90=
ENST00000562931.5:n.73C=
ENST00000566563.1:n.187C=
ENST00000567525.5:c.248-1436C= ENSP00000454484.1:n.248-1436C=
ENST00000568613.5:c.604C= ENSP00000457921.1:n.604C=
NM_000512.4:c.485C= NP_000503.1:p.Ser162=
XM_005256301.2:c.485C= XP_005256358.1:p.Ser162=
XM_005256302.1:c.503C= XP_005256359.1:p.Ser168=
XM_011522982.1:c.503C= XP_011521284.1:p.Ser168=
XM_011522984.1:c.503C= XP_011521286.1:p.Ser168=
NM_001323543.1:c.-71C= NP_001310472.1:n.-71C=
NM_001323544.1:c.503C= NP_001310473.1:p.Ser168=
XM_005256301.3:c.485C= XP_005256358.1:p.Ser162=
XM_011522982.2:c.503C= XP_011521284.1:p.Ser168=
XM_017023111.2:c.503C= XP_016878600.1:p.Ser168=
XM_017023112.2:c.503C= XP_016878601.1:p.Ser168=
XM_017023113.1:c.-71C= XP_016878602.1:n.-71C=
NM_000512.5:c.485C= MANE Select NP_000503.1:p.Ser162=
NM_001323543.2:c.-71C= NP_001310472.1:n.-71C=
NM_001323544.2:c.503C= NP_001310473.1:p.Ser168=