Canonical Allele Identifier: CA2241313250
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88817985C= , CM000678.2:g.88817985C= GRCh38
NC_000016.9:g.88884393C= , CM000678.1:g.88884393C= GRCh37
NC_000016.8:g.87411894C= NCBI36
NG_008667.1:g.43982G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.1482+22G= MANE Select ENSP00000268695.5:n.1482+22G=
ENST00000268695.9:c.1482+22G= ENSP00000268695.5:n.1482+22G=
ENST00000562593.5:n.4891+22G=
ENST00000567525.5:c.1163+22G= ENSP00000454484.1:n.1163+22G=
ENST00000568613.5:c.1601+22G= ENSP00000457921.1:n.1601+22G=
NM_000512.4:c.1482+22G= NP_000503.1:n.1482+22G=
XM_005256301.2:c.1482+22G= XP_005256358.1:n.1482+22G=
XM_005256302.1:c.1500+22G= XP_005256359.1:n.1500+22G=
XM_011522982.1:c.1500+22G= XP_011521284.1:n.1500+22G=
XM_011522984.1:c.1500+22G= XP_011521286.1:n.1500+22G=
NM_001323543.1:c.927+22G= NP_001310472.1:n.927+22G=
NM_001323544.1:c.1500+22G= NP_001310473.1:n.1500+22G=
XM_005256301.3:c.1482+22G= XP_005256358.1:n.1482+22G=
XM_011522982.2:c.1500+22G= XP_011521284.1:n.1500+22G=
XM_017023111.2:c.1500+22G= XP_016878600.1:n.1500+22G=
XM_017023112.2:c.1500+22G= XP_016878601.1:n.1500+22G=
XM_017023113.1:c.927+22G= XP_016878602.1:n.927+22G=
NM_000512.5:c.1482+22G= MANE Select NP_000503.1:n.1482+22G=
NM_001323543.2:c.927+22G= NP_001310472.1:n.927+22G=
NM_001323544.2:c.1500+22G= NP_001310473.1:n.1500+22G=