Canonical Allele Identifier: CA2688683138
Gene: ST3GAL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133475602_133475658del , CM000670.2:g.133475602_133475658del GRCh38
NC_000008.10:g.134487845_134487901del , CM000670.1:g.134487845_134487901del GRCh37
NC_000008.9:g.134557027_134557083del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000522652.6:c.306+73_306+129del MANE Select ENSP00000430515.1:n.306+73_306+129del
ENST00000648219.1:c.306+73_306+129del ENSP00000497381.1:n.306+73_306+129del
ENST00000399640.3:c.306+73_306+129del ENSP00000414073.1:n.306+73_306+129del
ENST00000517668.5:c.-84-9556_-84-9500del ENSP00000427720.1:n.-84-9556_-84-9500del
ENST00000521180.5:c.306+73_306+129del ENSP00000428540.1:n.306+73_306+129del
ENST00000522204.1:n.216+73_216+129del
ENST00000522652.5:c.306+73_306+129del ENSP00000430515.1:n.306+73_306+129del
ENST00000523854.5:c.-84-9556_-84-9500del ENSP00000429638.1:n.-84-9556_-84-9500del
NM_003033.3:c.306+73_306+129del NP_003024.1:n.306+73_306+129del
NM_173344.2:c.306+73_306+129del NP_775479.1:n.306+73_306+129del
XM_005251023.1:c.306+73_306+129del XP_005251080.1:n.306+73_306+129del
XM_005251024.3:c.306+73_306+129del XP_005251081.1:n.306+73_306+129del
XM_005251025.3:c.306+73_306+129del XP_005251082.1:n.306+73_306+129del
XM_006716617.1:c.306+73_306+129del XP_006716680.1:n.306+73_306+129del
XM_011517225.1:c.306+73_306+129del XP_011515527.1:n.306+73_306+129del
XM_011517226.1:c.306+73_306+129del XP_011515528.1:n.306+73_306+129del
XM_005251025.5:c.306+73_306+129del XP_005251082.1:n.306+73_306+129del
XM_006716617.2:c.306+73_306+129del XP_006716680.1:n.306+73_306+129del
XM_011517225.2:c.306+73_306+129del XP_011515527.1:n.306+73_306+129del
XM_017013736.2:c.306+73_306+129del XP_016869225.1:n.306+73_306+129del
XM_024447233.1:c.306+73_306+129del XP_024303001.1:n.306+73_306+129del
NM_173344.3:c.306+73_306+129del MANE Select NP_775479.1:n.306+73_306+129del
NM_003033.4:c.306+73_306+129del NP_003024.1:n.306+73_306+129del