Canonical Allele Identifier: CA2241328658
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88841966C= , CM000678.2:g.88841966C= GRCh38
NC_000016.9:g.88908374C= , CM000678.1:g.88908374C= GRCh37
NC_000016.8:g.87435875C= NCBI36
NG_008667.1:g.20001G=

Transcript Alleles

HGVS Amino-acid change
ENST00000268695.10:c.250G= MANE Select ENSP00000268695.5:p.Ala84=
ENST00000268695.9:c.250G= ENSP00000268695.5:p.Ala84=
ENST00000562593.5:n.3659G=
ENST00000562831.1:c.34G= ENSP00000455174.1:p.Ala12=
ENST00000565364.1:n.385G=
ENST00000567525.5:c.75G= ENSP00000454484.1:p.Gly25=
ENST00000567779.1:n.80G=
ENST00000568613.5:c.369G= ENSP00000457921.1:n.369G=
NM_000512.4:c.250G= NP_000503.1:p.Ala84=
XM_005256301.2:c.250G= XP_005256358.1:p.Ala84=
XM_005256302.1:c.268G= XP_005256359.1:p.Ala90=
XM_011522982.1:c.268G= XP_011521284.1:p.Ala90=
XM_011522984.1:c.268G= XP_011521286.1:p.Ala90=
NM_001323543.1:c.-306G= NP_001310472.1:n.-306G=
NM_001323544.1:c.268G= NP_001310473.1:p.Ala90=
XM_005256301.3:c.250G= XP_005256358.1:p.Ala84=
XM_011522982.2:c.268G= XP_011521284.1:p.Ala90=
XM_017023111.2:c.268G= XP_016878600.1:p.Ala90=
XM_017023112.2:c.268G= XP_016878601.1:p.Ala90=
XM_017023113.1:c.-306G= XP_016878602.1:n.-306G=
NM_000512.5:c.250G= MANE Select NP_000503.1:p.Ala84=
NM_001323543.2:c.-306G= NP_001310472.1:n.-306G=
NM_001323544.2:c.268G= NP_001310473.1:p.Ala90=