Canonical Allele Identifier: CA463035373
Gene: ST3GAL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.134474154G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133461911G>A , CM000670.2:g.133461911G>A GRCh38
NC_000008.10:g.134474154G>A , CM000670.1:g.134474154G>A GRCh37
NC_000008.9:g.134543336G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000522652.6:c.813C>T MANE Select ENSP00000430515.1:p.Ile271=
ENST00000648219.1:c.813C>T ENSP00000497381.1:p.Ile271=
ENST00000399640.3:c.813C>T ENSP00000414073.1:p.Ile271=
ENST00000521180.5:c.813C>T ENSP00000428540.1:p.Ile271=
ENST00000522652.5:c.813C>T ENSP00000430515.1:p.Ile271=
NM_003033.3:c.813C>T NP_003024.1:p.Ile271=
NM_173344.2:c.813C>T NP_775479.1:p.Ile271=
XM_005251023.1:c.813C>T XP_005251080.1:p.Ile271=
XM_005251024.3:c.813C>T XP_005251081.1:p.Ile271=
XM_005251025.3:c.813C>T XP_005251082.1:p.Ile271=
XM_006716617.1:c.813C>T XP_006716680.1:p.Ile271=
XM_011517225.1:c.813C>T XP_011515527.1:p.Ile271=
XM_011517226.1:c.813C>T XP_011515528.1:p.Ile271=
XM_005251025.5:c.813C>T XP_005251082.1:p.Ile271=
XM_006716617.2:c.813C>T XP_006716680.1:p.Ile271=
XM_011517225.2:c.813C>T XP_011515527.1:p.Ile271=
XM_017013736.2:c.813C>T XP_016869225.1:p.Ile271=
XM_024447233.1:c.813C>T XP_024303001.1:p.Ile271=
NM_173344.3:c.813C>T MANE Select NP_775479.1:p.Ile271=
NM_003033.4:c.813C>T NP_003024.1:p.Ile271=