Canonical Allele Identifier: CA4887269

Gene: ST3GAL1

Linked Data

• dbSNP Id: rs145807165
• ExAC: 8:134487995 C / T
• gnomAD v2: 8-134487995-C-T
• gnomAD v3: 8-133475752-C-T
• gnomAD v4: 8-133475752-C-T
• MyVariant Identifiers: chr8:g.134487995C>T (hg19) ; chr8:g.133475752C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133475752C>T , CM000670.2:g.133475752C>T	GRCh38
NC_000008.10:g.134487995C>T , CM000670.1:g.134487995C>T	GRCh37
NC_000008.9:g.134557177C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000522652.6:c.273G>A MANE Select	ENSP00000430515.1:p.Ala91=
ENST00000648219.1:c.273G>A	ENSP00000497381.1:p.Ala91=
ENST00000399640.3:c.273G>A	ENSP00000414073.1:p.Ala91=
ENST00000517668.5:c.-84-9662G>A	ENSP00000427720.1:n.-84-9662G>A
ENST00000521180.5:c.273G>A	ENSP00000428540.1:p.Ala91=
ENST00000522204.1:n.183G>A
ENST00000522652.5:c.273G>A	ENSP00000430515.1:p.Ala91=
ENST00000523854.5:c.-84-9662G>A	ENSP00000429638.1:n.-84-9662G>A
NM_003033.3:c.273G>A	NP_003024.1:p.Ala91=
NM_173344.2:c.273G>A	NP_775479.1:p.Ala91=
XM_005251023.1:c.273G>A	XP_005251080.1:p.Ala91=
XM_005251024.3:c.273G>A	XP_005251081.1:p.Ala91=
XM_005251025.3:c.273G>A	XP_005251082.1:p.Ala91=
XM_006716617.1:c.273G>A	XP_006716680.1:p.Ala91=
XM_011517225.1:c.273G>A	XP_011515527.1:p.Ala91=
XM_011517226.1:c.273G>A	XP_011515528.1:p.Ala91=
XM_005251025.5:c.273G>A	XP_005251082.1:p.Ala91=
XM_006716617.2:c.273G>A	XP_006716680.1:p.Ala91=
XM_011517225.2:c.273G>A	XP_011515527.1:p.Ala91=
XM_017013736.2:c.273G>A	XP_016869225.1:p.Ala91=
XM_024447233.1:c.273G>A	XP_024303001.1:p.Ala91=
NM_173344.3:c.273G>A MANE Select	NP_775479.1:p.Ala91=
NM_003033.4:c.273G>A	NP_003024.1:p.Ala91=