Canonical Allele Identifier: CA4887072

Gene: ST3GAL1

Linked Data

• dbSNP Id: rs750841491
• ExAC: 8:134474151 G / A
• gnomAD v2: 8-134474151-G-A
• gnomAD v4: 8-133461908-G-A
• MyVariant Identifiers: chr8:g.134474151G>A (hg19) ; chr8:g.133461908G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133461908G>A , CM000670.2:g.133461908G>A	GRCh38
NC_000008.10:g.134474151G>A , CM000670.1:g.134474151G>A	GRCh37
NC_000008.9:g.134543333G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000522652.6:c.816C>T MANE Select	ENSP00000430515.1:p.Leu272=
ENST00000648219.1:c.816C>T	ENSP00000497381.1:p.Leu272=
ENST00000399640.3:c.816C>T	ENSP00000414073.1:p.Leu272=
ENST00000521180.5:c.816C>T	ENSP00000428540.1:p.Leu272=
ENST00000522652.5:c.816C>T	ENSP00000430515.1:p.Leu272=
NM_003033.3:c.816C>T	NP_003024.1:p.Leu272=
NM_173344.2:c.816C>T	NP_775479.1:p.Leu272=
XM_005251023.1:c.816C>T	XP_005251080.1:p.Leu272=
XM_005251024.3:c.816C>T	XP_005251081.1:p.Leu272=
XM_005251025.3:c.816C>T	XP_005251082.1:p.Leu272=
XM_006716617.1:c.816C>T	XP_006716680.1:p.Leu272=
XM_011517225.1:c.816C>T	XP_011515527.1:p.Leu272=
XM_011517226.1:c.816C>T	XP_011515528.1:p.Leu272=
XM_005251025.5:c.816C>T	XP_005251082.1:p.Leu272=
XM_006716617.2:c.816C>T	XP_006716680.1:p.Leu272=
XM_011517225.2:c.816C>T	XP_011515527.1:p.Leu272=
XM_017013736.2:c.816C>T	XP_016869225.1:p.Leu272=
XM_024447233.1:c.816C>T	XP_024303001.1:p.Leu272=
NM_173344.3:c.816C>T MANE Select	NP_775479.1:p.Leu272=
NM_003033.4:c.816C>T	NP_003024.1:p.Leu272=