Canonical Allele Identifier: CA347533917
Gene: ST3GAL5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85861183T>A , CM000664.2:g.85861183T>A GRCh38
NC_000002.11:g.86088306T>A , CM000664.1:g.86088306T>A GRCh37
NC_000002.10:g.85941817T>A NCBI36
NG_012807.1:g.32852A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306262.10:c.*60A>T ENSP00000306247.6:n.*60A>T
ENST00000377332.8:c.316A>T ENSP00000366549.4:p.Lys106Ter
ENST00000393805.6:c.232A>T ENSP00000377394.1:p.Lys78Ter
ENST00000393808.8:c.247A>T ENSP00000377397.3:p.Lys83Ter
ENST00000433665.6:c.*359A>T ENSP00000408635.1:n.*359A>T
ENST00000461199.6:n.768A>T
ENST00000461892.6:n.321A>T
ENST00000473122.6:c.316A>T ENSP00000491314.1:p.Lys106Ter
ENST00000484728.6:n.327A>T
ENST00000638178.1:c.232A>T ENSP00000492103.1:p.Lys78Ter
ENST00000638227.1:c.*359A>T ENSP00000492602.1:n.*359A>T
ENST00000638288.1:c.232A>T ENSP00000491699.1:p.Lys78Ter
ENST00000638321.1:c.213A>T
ENST00000638484.1:c.*359A>T ENSP00000492635.1:n.*359A>T
ENST00000638523.1:c.213A>T
ENST00000638542.1:c.206+2179A>T ENSP00000492468.1:n.206+2179A>T
ENST00000638572.2:c.316A>T MANE Select ENSP00000491316.1:p.Lys106Ter
ENST00000638581.1:n.342A>T
ENST00000638659.1:c.502A>T
ENST00000638678.1:c.314A>T
ENST00000638855.1:c.206+2179A>T ENSP00000490979.1:n.206+2179A>T
ENST00000638885.1:c.316A>T ENSP00000492209.1:p.Lys106Ter
ENST00000638956.1:c.316A>T ENSP00000492097.1:p.Lys106Ter
ENST00000638986.1:c.232A>T ENSP00000491853.1:p.Lys78Ter
ENST00000639119.1:c.316A>T ENSP00000492045.1:p.Lys106Ter
ENST00000639184.1:c.232A>T ENSP00000492305.1:p.Lys78Ter
ENST00000639202.1:c.199A>T ENSP00000492710.1:p.Lys67Ter
ENST00000639216.1:n.338A>T
ENST00000639305.1:c.314A>T
ENST00000639311.1:c.316A>T ENSP00000491398.1:p.Lys106Ter
ENST00000639421.1:c.503A>T ENSP00000491029.1:n.503A>T
ENST00000639432.1:c.232A>T ENSP00000491828.1:p.Lys78Ter
ENST00000639519.1:c.118A>T ENSP00000491857.1:p.Lys40Ter
ENST00000639541.1:c.316A>T ENSP00000492280.1:p.Lys106Ter
ENST00000639608.1:c.316A>T ENSP00000492473.1:p.Lys106Ter
ENST00000639690.1:c.416A>T ENSP00000491917.1:n.416A>T
ENST00000639820.1:c.*573A>T ENSP00000491802.1:n.*573A>T
ENST00000639945.1:c.316A>T ENSP00000492866.1:p.Lys106Ter
ENST00000639981.1:c.222A>T
ENST00000640024.1:c.316A>T ENSP00000491238.1:p.Lys106Ter
ENST00000640222.1:c.237A>T
ENST00000640295.1:c.503A>T ENSP00000491027.1:n.503A>T
ENST00000640314.1:c.479A>T ENSP00000491315.1:n.479A>T
ENST00000640315.1:c.292A>T ENSP00000492089.1:p.Lys98Ter
ENST00000640322.1:c.232A>T ENSP00000491564.1:p.Lys78Ter
ENST00000640378.1:c.49A>T ENSP00000492030.1:p.Lys17Ter
ENST00000640418.1:c.373A>T ENSP00000492098.1:p.Lys125Ter
ENST00000640425.1:c.299A>T
ENST00000640572.1:c.299A>T
ENST00000640594.1:c.*359A>T ENSP00000491356.1:n.*359A>T
ENST00000640763.1:c.35A>T
ENST00000640835.1:c.198A>T
ENST00000640849.1:c.211A>T ENSP00000491701.1:p.Lys71Ter
ENST00000640903.1:c.402A>T
ENST00000640982.1:c.232A>T ENSP00000492299.1:p.Lys78Ter
ENST00000640992.1:c.232A>T ENSP00000492753.1:p.Lys78Ter
ENST00000306262.9:c.316A>T ENSP00000306247.5:p.Lys106Ter
ENST00000377332.7:c.316A>T ENSP00000366549.3:p.Lys106Ter
ENST00000393805.5:c.232A>T ENSP00000377394.1:p.Lys78Ter
ENST00000393808.7:c.247A>T ENSP00000377397.3:p.Lys83Ter
ENST00000433665.5:c.*359A>T ENSP00000408635.1:n.*359A>T
ENST00000455892.1:c.232A>T ENSP00000401375.1:p.Lys78Ter
ENST00000461199.5:n.321A>T
ENST00000461892.5:n.319A>T
ENST00000473122.5:n.288A>T
ENST00000484728.5:n.322A>T
NM_001042437.1:c.247A>T NP_001035902.1:p.Lys83Ter
NM_003896.3:c.316A>T NP_003887.3:p.Lys106Ter
XM_005264630.3:c.316A>T XP_005264687.1:p.Lys106Ter
XM_011533143.1:c.-246A>T XP_011531445.1:n.-246A>T
XR_939734.1:n.401A>T
XR_939735.1:n.401A>T
XR_939736.1:n.401A>T
NM_001354223.1:c.-246A>T NP_001341152.1:n.-246A>T
NM_001354224.1:c.-309A>T NP_001341153.1:n.-309A>T
NM_001354226.1:c.-246A>T NP_001341155.1:n.-246A>T
NM_001354227.1:c.232A>T NP_001341156.1:p.Lys78Ter
NM_001354229.1:c.232A>T NP_001341158.1:p.Lys78Ter
NM_001354233.1:c.-686A>T NP_001341162.1:n.-686A>T
NM_001354234.1:c.-650A>T NP_001341163.1:n.-650A>T
NM_001354238.1:c.232A>T NP_001341167.1:p.Lys78Ter
NM_001363847.1:c.316A>T NP_001350776.1:p.Lys106Ter
XM_017005202.2:c.232A>T XP_016860691.1:p.Lys78Ter
XM_017005203.2:c.-749A>T XP_016860692.1:n.-749A>T
XM_017005204.2:c.-749A>T XP_016860693.1:n.-749A>T
XM_017005205.2:c.-741A>T XP_016860694.1:n.-741A>T
XM_017005206.2:c.-650A>T XP_016860695.1:n.-650A>T
XM_017005208.2:c.-650A>T XP_016860697.1:n.-650A>T
XM_017005209.1:c.-301A>T XP_016860698.1:n.-301A>T
XM_017005212.2:c.-210A>T XP_016860701.1:n.-210A>T
XM_017005214.2:c.-246A>T XP_016860703.1:n.-246A>T
XR_001739019.1:n.401A>T
XR_001739020.1:n.401A>T
XR_001739021.1:n.401A>T
NM_003896.4:c.316A>T MANE Select NP_003887.3:p.Lys106Ter
NM_001042437.2:c.247A>T NP_001035902.1:p.Lys83Ter
NM_001354223.2:c.-246A>T NP_001341152.1:n.-246A>T
NM_001354224.2:c.-309A>T NP_001341153.1:n.-309A>T
NM_001354226.2:c.-246A>T NP_001341155.1:n.-246A>T
NM_001354227.2:c.232A>T NP_001341156.1:p.Lys78Ter
NM_001354229.2:c.232A>T NP_001341158.1:p.Lys78Ter
NM_001354233.2:c.-686A>T NP_001341162.1:n.-686A>T