Canonical Allele Identifier: CA2688683222

Gene: ST3GAL1

Linked Data

• gnomAD v4: 8-133475661-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133475661C>A , CM000670.2:g.133475661C>A	GRCh38
NC_000008.10:g.134487904C>A , CM000670.1:g.134487904C>A	GRCh37
NC_000008.9:g.134557086C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000522652.6:c.306+58G>T MANE Select	ENSP00000430515.1:n.306+58G>T
ENST00000648219.1:c.306+58G>T	ENSP00000497381.1:n.306+58G>T
ENST00000399640.3:c.306+58G>T	ENSP00000414073.1:n.306+58G>T
ENST00000517668.5:c.-84-9571G>T	ENSP00000427720.1:n.-84-9571G>T
ENST00000521180.5:c.306+58G>T	ENSP00000428540.1:n.306+58G>T
ENST00000522204.1:n.216+58G>T
ENST00000522652.5:c.306+58G>T	ENSP00000430515.1:n.306+58G>T
ENST00000523854.5:c.-84-9571G>T	ENSP00000429638.1:n.-84-9571G>T
NM_003033.3:c.306+58G>T	NP_003024.1:n.306+58G>T
NM_173344.2:c.306+58G>T	NP_775479.1:n.306+58G>T
XM_005251023.1:c.306+58G>T	XP_005251080.1:n.306+58G>T
XM_005251024.3:c.306+58G>T	XP_005251081.1:n.306+58G>T
XM_005251025.3:c.306+58G>T	XP_005251082.1:n.306+58G>T
XM_006716617.1:c.306+58G>T	XP_006716680.1:n.306+58G>T
XM_011517225.1:c.306+58G>T	XP_011515527.1:n.306+58G>T
XM_011517226.1:c.306+58G>T	XP_011515528.1:n.306+58G>T
XM_005251025.5:c.306+58G>T	XP_005251082.1:n.306+58G>T
XM_006716617.2:c.306+58G>T	XP_006716680.1:n.306+58G>T
XM_011517225.2:c.306+58G>T	XP_011515527.1:n.306+58G>T
XM_017013736.2:c.306+58G>T	XP_016869225.1:n.306+58G>T
XM_024447233.1:c.306+58G>T	XP_024303001.1:n.306+58G>T
NM_173344.3:c.306+58G>T MANE Select	NP_775479.1:n.306+58G>T
NM_003033.4:c.306+58G>T	NP_003024.1:n.306+58G>T