Canonical Allele Identifier: CA1821262867
Gene: ST3GAL1 HGNC NCBI

Linked Data

dbSNP Id: rs1815531524

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133462037dup , CM000670.2:g.133462037dup GRCh38
NC_000008.10:g.134474280dup , CM000670.1:g.134474280dup GRCh37
NC_000008.9:g.134543462dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000522652.6:c.730-38dup MANE Select ENSP00000430515.1:n.730-38dup
ENST00000648219.1:c.730-38dup ENSP00000497381.1:n.730-38dup
ENST00000399640.3:c.730-38dup ENSP00000414073.1:n.730-38dup
ENST00000521180.5:c.730-38dup ENSP00000428540.1:n.730-38dup
ENST00000522652.5:c.730-38dup ENSP00000430515.1:n.730-38dup
NM_003033.3:c.730-38dup NP_003024.1:n.730-38dup
NM_173344.2:c.730-38dup NP_775479.1:n.730-38dup
XM_005251023.1:c.730-38dup XP_005251080.1:n.730-38dup
XM_005251024.3:c.730-38dup XP_005251081.1:n.730-38dup
XM_005251025.3:c.730-38dup XP_005251082.1:n.730-38dup
XM_006716617.1:c.730-38dup XP_006716680.1:n.730-38dup
XM_011517225.1:c.730-38dup XP_011515527.1:n.730-38dup
XM_011517226.1:c.730-38dup XP_011515528.1:n.730-38dup
XM_005251025.5:c.730-38dup XP_005251082.1:n.730-38dup
XM_006716617.2:c.730-38dup XP_006716680.1:n.730-38dup
XM_011517225.2:c.730-38dup XP_011515527.1:n.730-38dup
XM_017013736.2:c.730-38dup XP_016869225.1:n.730-38dup
XM_024447233.1:c.730-38dup XP_024303001.1:n.730-38dup
NM_173344.3:c.730-38dup MANE Select NP_775479.1:n.730-38dup
NM_003033.4:c.730-38dup NP_003024.1:n.730-38dup