Canonical Allele Identifier: CA4887078
Gene: ST3GAL1 HGNC NCBI

Linked Data

dbSNP Id: rs746489251

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133461924G>T , CM000670.2:g.133461924G>T GRCh38
NC_000008.10:g.134474167G>T , CM000670.1:g.134474167G>T GRCh37
NC_000008.9:g.134543349G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000522652.6:c.800C>A MANE Select ENSP00000430515.1:p.Pro267Gln
ENST00000648219.1:c.800C>A ENSP00000497381.1:p.Pro267Gln
ENST00000399640.3:c.800C>A ENSP00000414073.1:p.Pro267Gln
ENST00000521180.5:c.800C>A ENSP00000428540.1:p.Pro267Gln
ENST00000522652.5:c.800C>A ENSP00000430515.1:p.Pro267Gln
NM_003033.3:c.800C>A NP_003024.1:p.Pro267Gln
NM_173344.2:c.800C>A NP_775479.1:p.Pro267Gln
XM_005251023.1:c.800C>A XP_005251080.1:p.Pro267Gln
XM_005251024.3:c.800C>A XP_005251081.1:p.Pro267Gln
XM_005251025.3:c.800C>A XP_005251082.1:p.Pro267Gln
XM_006716617.1:c.800C>A XP_006716680.1:p.Pro267Gln
XM_011517225.1:c.800C>A XP_011515527.1:p.Pro267Gln
XM_011517226.1:c.800C>A XP_011515528.1:p.Pro267Gln
XM_005251025.5:c.800C>A XP_005251082.1:p.Pro267Gln
XM_006716617.2:c.800C>A XP_006716680.1:p.Pro267Gln
XM_011517225.2:c.800C>A XP_011515527.1:p.Pro267Gln
XM_017013736.2:c.800C>A XP_016869225.1:p.Pro267Gln
XM_024447233.1:c.800C>A XP_024303001.1:p.Pro267Gln
NM_173344.3:c.800C>A MANE Select NP_775479.1:p.Pro267Gln
NM_003033.4:c.800C>A NP_003024.1:p.Pro267Gln