Canonical Allele Identifier: CA347533948
Gene: ST3GAL5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85861197T>C , CM000664.2:g.85861197T>C GRCh38
NC_000002.11:g.86088320T>C , CM000664.1:g.86088320T>C GRCh37
NC_000002.10:g.85941831T>C NCBI36
NG_012807.1:g.32838A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306262.10:c.*46A>G ENSP00000306247.6:n.*46A>G
ENST00000377332.8:c.302A>G ENSP00000366549.4:p.Asp101Gly
ENST00000393805.6:c.218A>G ENSP00000377394.1:p.Asp73Gly
ENST00000393808.8:c.233A>G ENSP00000377397.3:p.Asp78Gly
ENST00000433665.6:c.*345A>G ENSP00000408635.1:n.*345A>G
ENST00000461199.6:n.754A>G
ENST00000461892.6:n.307A>G
ENST00000473122.6:c.302A>G ENSP00000491314.1:p.Asp101Gly
ENST00000484728.6:n.313A>G
ENST00000638178.1:c.218A>G ENSP00000492103.1:p.Asp73Gly
ENST00000638227.1:c.*345A>G ENSP00000492602.1:n.*345A>G
ENST00000638288.1:c.218A>G ENSP00000491699.1:p.Asp73Gly
ENST00000638321.1:c.199A>G
ENST00000638484.1:c.*345A>G ENSP00000492635.1:n.*345A>G
ENST00000638523.1:c.199A>G
ENST00000638542.1:c.206+2165A>G ENSP00000492468.1:n.206+2165A>G
ENST00000638572.2:c.302A>G MANE Select ENSP00000491316.1:p.Asp101Gly
ENST00000638581.1:n.328A>G
ENST00000638659.1:c.488A>G
ENST00000638678.1:c.300A>G
ENST00000638855.1:c.206+2165A>G ENSP00000490979.1:n.206+2165A>G
ENST00000638885.1:c.302A>G ENSP00000492209.1:p.Asp101Gly
ENST00000638956.1:c.302A>G ENSP00000492097.1:p.Asp101Gly
ENST00000638986.1:c.218A>G ENSP00000491853.1:p.Asp73Gly
ENST00000639119.1:c.302A>G ENSP00000492045.1:p.Asp101Gly
ENST00000639184.1:c.218A>G ENSP00000492305.1:p.Asp73Gly
ENST00000639202.1:c.185A>G ENSP00000492710.1:p.Asp62Gly
ENST00000639216.1:n.324A>G
ENST00000639305.1:c.300A>G
ENST00000639311.1:c.302A>G ENSP00000491398.1:p.Asp101Gly
ENST00000639421.1:c.489A>G ENSP00000491029.1:n.489A>G
ENST00000639432.1:c.218A>G ENSP00000491828.1:p.Asp73Gly
ENST00000639519.1:c.104A>G ENSP00000491857.1:p.Asp35Gly
ENST00000639541.1:c.302A>G ENSP00000492280.1:p.Asp101Gly
ENST00000639608.1:c.302A>G ENSP00000492473.1:p.Asp101Gly
ENST00000639690.1:c.402A>G ENSP00000491917.1:n.402A>G
ENST00000639820.1:c.*559A>G ENSP00000491802.1:n.*559A>G
ENST00000639945.1:c.302A>G ENSP00000492866.1:p.Asp101Gly
ENST00000639981.1:c.208A>G
ENST00000640024.1:c.302A>G ENSP00000491238.1:p.Asp101Gly
ENST00000640222.1:c.223A>G
ENST00000640295.1:c.489A>G ENSP00000491027.1:n.489A>G
ENST00000640314.1:c.465A>G ENSP00000491315.1:n.465A>G
ENST00000640315.1:c.278A>G ENSP00000492089.1:p.Asp93Gly
ENST00000640322.1:c.218A>G ENSP00000491564.1:p.Asp73Gly
ENST00000640378.1:c.35A>G ENSP00000492030.1:p.Asp12Gly
ENST00000640418.1:c.359A>G ENSP00000492098.1:p.Asp120Gly
ENST00000640425.1:c.285A>G
ENST00000640572.1:c.285A>G
ENST00000640594.1:c.*345A>G ENSP00000491356.1:n.*345A>G
ENST00000640763.1:c.21A>G
ENST00000640835.1:c.184A>G
ENST00000640849.1:c.197A>G ENSP00000491701.1:p.Asp66Gly
ENST00000640903.1:c.388A>G
ENST00000640982.1:c.218A>G ENSP00000492299.1:p.Asp73Gly
ENST00000640992.1:c.218A>G ENSP00000492753.1:p.Asp73Gly
ENST00000306262.9:c.302A>G ENSP00000306247.5:p.Asp101Gly
ENST00000377332.7:c.302A>G ENSP00000366549.3:p.Asp101Gly
ENST00000393805.5:c.218A>G ENSP00000377394.1:p.Asp73Gly
ENST00000393808.7:c.233A>G ENSP00000377397.3:p.Asp78Gly
ENST00000433665.5:c.*345A>G ENSP00000408635.1:n.*345A>G
ENST00000455892.1:c.218A>G ENSP00000401375.1:p.Asp73Gly
ENST00000461199.5:n.307A>G
ENST00000461892.5:n.305A>G
ENST00000473122.5:n.274A>G
ENST00000484728.5:n.308A>G
NM_001042437.1:c.233A>G NP_001035902.1:p.Asp78Gly
NM_003896.3:c.302A>G NP_003887.3:p.Asp101Gly
XM_005264630.3:c.302A>G XP_005264687.1:p.Asp101Gly
XM_011533143.1:c.-260A>G XP_011531445.1:n.-260A>G
XR_939734.1:n.387A>G
XR_939735.1:n.387A>G
XR_939736.1:n.387A>G
NM_001354223.1:c.-260A>G NP_001341152.1:n.-260A>G
NM_001354224.1:c.-323A>G NP_001341153.1:n.-323A>G
NM_001354226.1:c.-260A>G NP_001341155.1:n.-260A>G
NM_001354227.1:c.218A>G NP_001341156.1:p.Asp73Gly
NM_001354229.1:c.218A>G NP_001341158.1:p.Asp73Gly
NM_001354233.1:c.-700A>G NP_001341162.1:n.-700A>G
NM_001354234.1:c.-664A>G NP_001341163.1:n.-664A>G
NM_001354238.1:c.218A>G NP_001341167.1:p.Asp73Gly
NM_001363847.1:c.302A>G NP_001350776.1:p.Asp101Gly
XM_017005202.2:c.218A>G XP_016860691.1:p.Asp73Gly
XM_017005203.2:c.-763A>G XP_016860692.1:n.-763A>G
XM_017005204.2:c.-763A>G XP_016860693.1:n.-763A>G
XM_017005205.2:c.-755A>G XP_016860694.1:n.-755A>G
XM_017005206.2:c.-664A>G XP_016860695.1:n.-664A>G
XM_017005208.2:c.-664A>G XP_016860697.1:n.-664A>G
XM_017005209.1:c.-315A>G XP_016860698.1:n.-315A>G
XM_017005212.2:c.-224A>G XP_016860701.1:n.-224A>G
XM_017005214.2:c.-260A>G XP_016860703.1:n.-260A>G
XR_001739019.1:n.387A>G
XR_001739020.1:n.387A>G
XR_001739021.1:n.387A>G
NM_003896.4:c.302A>G MANE Select NP_003887.3:p.Asp101Gly
NM_001042437.2:c.233A>G NP_001035902.1:p.Asp78Gly
NM_001354223.2:c.-260A>G NP_001341152.1:n.-260A>G
NM_001354224.2:c.-323A>G NP_001341153.1:n.-323A>G
NM_001354226.2:c.-260A>G NP_001341155.1:n.-260A>G
NM_001354227.2:c.218A>G NP_001341156.1:p.Asp73Gly
NM_001354229.2:c.218A>G NP_001341158.1:p.Asp73Gly
NM_001354233.2:c.-700A>G NP_001341162.1:n.-700A>G