Canonical Allele Identifier: CA186411555

Gene: ST3GAL1

Linked Data

• dbSNP Id: rs931855703
• gnomAD v4: 8-133461815-T-G
• MyVariant Identifiers: chr8:g.133461815T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133461815T>G , CM000670.2:g.133461815T>G	GRCh38
NC_000008.10:g.134474058T>G , CM000670.1:g.134474058T>G	GRCh37
NC_000008.9:g.134543240T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000522652.6:c.849+60A>C MANE Select	ENSP00000430515.1:n.849+60A>C
ENST00000648219.1:c.849+60A>C	ENSP00000497381.1:n.849+60A>C
ENST00000399640.3:c.849+60A>C	ENSP00000414073.1:n.849+60A>C
ENST00000521180.5:c.849+60A>C	ENSP00000428540.1:n.849+60A>C
ENST00000522652.5:c.849+60A>C	ENSP00000430515.1:n.849+60A>C
NM_003033.3:c.849+60A>C	NP_003024.1:n.849+60A>C
NM_173344.2:c.849+60A>C	NP_775479.1:n.849+60A>C
XM_005251023.1:c.849+60A>C	XP_005251080.1:n.849+60A>C
XM_005251024.3:c.849+60A>C	XP_005251081.1:n.849+60A>C
XM_005251025.3:c.849+60A>C	XP_005251082.1:n.849+60A>C
XM_006716617.1:c.849+60A>C	XP_006716680.1:n.849+60A>C
XM_011517225.1:c.849+60A>C	XP_011515527.1:n.849+60A>C
XM_011517226.1:c.849+60A>C	XP_011515528.1:n.849+60A>C
XM_005251025.5:c.849+60A>C	XP_005251082.1:n.849+60A>C
XM_006716617.2:c.849+60A>C	XP_006716680.1:n.849+60A>C
XM_011517225.2:c.849+60A>C	XP_011515527.1:n.849+60A>C
XM_017013736.2:c.849+60A>C	XP_016869225.1:n.849+60A>C
XM_024447233.1:c.849+60A>C	XP_024303001.1:n.849+60A>C
NM_173344.3:c.849+60A>C MANE Select	NP_775479.1:n.849+60A>C
NM_003033.4:c.849+60A>C	NP_003024.1:n.849+60A>C