Canonical Allele Identifier: CA13473833
Gene: ST3GAL4 HGNC NCBI

Linked Data

dbSNP Id: rs4937126
gnomAD v2: 11-126281897-G-A
gnomAD v3: 11-126412002-G-A
gnomAD v4: 11-126412002-G-A
MyVariant Identifiers: chr11:g.126281897G>A (hg19) chr11:g.126412002G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126412002G>A , CM000673.2:g.126412002G>A GRCh38
NC_000011.9:g.126281897G>A , CM000673.1:g.126281897G>A GRCh37
NC_000011.8:g.125787107G>A NCBI36
NG_053025.1:g.61358G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356132.9:c.835-1503G>A ENSP00000348451.5:n.835-1503G>A
ENST00000444328.7:c.772-1503G>A MANE Select ENSP00000394354.2:n.772-1503G>A
ENST00000676831.1:n.967-1503G>A
ENST00000676867.1:c.772-1328G>A ENSP00000503991.1:n.772-1328G>A
ENST00000677503.1:c.760-1585G>A ENSP00000504548.1:n.760-1585G>A
ENST00000677721.1:c.*36-1503G>A ENSP00000502908.1:n.*36-1503G>A
ENST00000678865.1:c.772-1585G>A ENSP00000504245.1:n.772-1585G>A
ENST00000227495.10:c.760-1503G>A ENSP00000227495.6:n.760-1503G>A
ENST00000356132.8:c.790-1503G>A ENSP00000348451.4:n.790-1503G>A
ENST00000392669.6:c.772-1503G>A ENSP00000376437.2:n.772-1503G>A
ENST00000444328.6:c.772-1503G>A ENSP00000394354.2:n.772-1503G>A
ENST00000449406.6:c.739-1503G>A ENSP00000399444.2:n.739-1503G>A
ENST00000524834.5:n.629+2591G>A
ENST00000524860.1:c.280-1503G>A ENSP00000431170.1:n.280-1503G>A
ENST00000526727.5:c.772-1503G>A ENSP00000436047.1:n.772-1503G>A
ENST00000530591.5:c.760-1503G>A ENSP00000433989.1:n.760-1503G>A
ENST00000531217.5:c.*330-1503G>A ENSP00000432929.1:n.*330-1503G>A
ENST00000532243.5:c.769-1503G>A ENSP00000434349.1:n.769-1503G>A
ENST00000533826.1:n.192-1395G>A
ENST00000534083.5:c.772-1503G>A ENSP00000433318.1:n.772-1503G>A
ENST00000534457.5:c.757-1503G>A ENSP00000434668.1:n.757-1503G>A
NM_001254757.1:c.772-1503G>A NP_001241686.1:n.772-1503G>A
NM_001254758.1:c.772-1503G>A NP_001241687.1:n.772-1503G>A
NM_001254759.1:c.769-1503G>A NP_001241688.1:n.769-1503G>A
NM_006278.2:c.760-1503G>A NP_006269.1:n.760-1503G>A
XM_011542959.1:c.771+2591G>A XP_011541261.1:n.771+2591G>A
XM_011542960.1:c.771+2591G>A XP_011541262.1:n.771+2591G>A
XM_011542961.1:c.771+2591G>A XP_011541263.1:n.771+2591G>A
XM_011542962.1:c.771+2591G>A XP_011541264.1:n.771+2591G>A
NM_001348396.1:c.835-1503G>A NP_001335325.1:n.835-1503G>A
NM_001348397.1:c.835-1503G>A NP_001335326.1:n.835-1503G>A
NM_001348398.1:c.760-1585G>A NP_001335327.1:n.760-1585G>A
NM_001348399.1:c.772-1503G>A NP_001335328.1:n.772-1503G>A
NM_001348400.1:c.760-1503G>A NP_001335329.1:n.760-1503G>A
NR_145671.1:n.1030-1328G>A
XM_024448658.1:c.772-1503G>A XP_024304426.1:n.772-1503G>A
XM_024448659.1:c.772-1503G>A XP_024304427.1:n.772-1503G>A
XM_024448660.1:c.772-1503G>A XP_024304428.1:n.772-1503G>A
NM_001254757.2:c.772-1503G>A MANE Select NP_001241686.1:n.772-1503G>A
NM_001254759.2:c.769-1503G>A NP_001241688.1:n.769-1503G>A
NM_001348396.2:c.835-1503G>A NP_001335325.1:n.835-1503G>A
NM_001348397.2:c.835-1503G>A NP_001335326.1:n.835-1503G>A
NM_001348398.2:c.760-1585G>A NP_001335327.1:n.760-1585G>A
NM_001348399.2:c.772-1503G>A NP_001335328.1:n.772-1503G>A
NM_001348400.2:c.760-1503G>A NP_001335329.1:n.760-1503G>A
NM_006278.3:c.760-1503G>A NP_006269.1:n.760-1503G>A
NR_145671.2:n.989-1328G>A
NM_001254758.2:c.772-1503G>A NP_001241687.1:n.772-1503G>A
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