Canonical Allele Identifier: CA347533916
Gene: ST3GAL5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85861182T>G , CM000664.2:g.85861182T>G GRCh38
NC_000002.11:g.86088305T>G , CM000664.1:g.86088305T>G GRCh37
NC_000002.10:g.85941816T>G NCBI36
NG_012807.1:g.32853A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000306262.10:c.*61A>C ENSP00000306247.6:n.*61A>C
ENST00000377332.8:c.317A>C ENSP00000366549.4:p.Lys106Thr
ENST00000393805.6:c.233A>C ENSP00000377394.1:p.Lys78Thr
ENST00000393808.8:c.248A>C ENSP00000377397.3:p.Lys83Thr
ENST00000433665.6:c.*360A>C ENSP00000408635.1:n.*360A>C
ENST00000461199.6:n.769A>C
ENST00000461892.6:n.322A>C
ENST00000473122.6:c.317A>C ENSP00000491314.1:p.Lys106Thr
ENST00000484728.6:n.328A>C
ENST00000638178.1:c.233A>C ENSP00000492103.1:p.Lys78Thr
ENST00000638227.1:c.*360A>C ENSP00000492602.1:n.*360A>C
ENST00000638288.1:c.233A>C ENSP00000491699.1:p.Lys78Thr
ENST00000638321.1:c.214A>C
ENST00000638484.1:c.*360A>C ENSP00000492635.1:n.*360A>C
ENST00000638523.1:c.214A>C
ENST00000638542.1:c.206+2180A>C ENSP00000492468.1:n.206+2180A>C
ENST00000638572.2:c.317A>C MANE Select ENSP00000491316.1:p.Lys106Thr
ENST00000638581.1:n.343A>C
ENST00000638659.1:c.503A>C
ENST00000638678.1:c.315A>C
ENST00000638855.1:c.206+2180A>C ENSP00000490979.1:n.206+2180A>C
ENST00000638885.1:c.317A>C ENSP00000492209.1:p.Lys106Thr
ENST00000638956.1:c.317A>C ENSP00000492097.1:p.Lys106Thr
ENST00000638986.1:c.233A>C ENSP00000491853.1:p.Lys78Thr
ENST00000639119.1:c.317A>C ENSP00000492045.1:p.Lys106Thr
ENST00000639184.1:c.233A>C ENSP00000492305.1:p.Lys78Thr
ENST00000639202.1:c.200A>C ENSP00000492710.1:p.Lys67Thr
ENST00000639216.1:n.339A>C
ENST00000639305.1:c.315A>C
ENST00000639311.1:c.317A>C ENSP00000491398.1:p.Lys106Thr
ENST00000639421.1:c.504A>C ENSP00000491029.1:n.504A>C
ENST00000639432.1:c.233A>C ENSP00000491828.1:p.Lys78Thr
ENST00000639519.1:c.119A>C ENSP00000491857.1:p.Lys40Thr
ENST00000639541.1:c.317A>C ENSP00000492280.1:p.Lys106Thr
ENST00000639608.1:c.317A>C ENSP00000492473.1:p.Lys106Thr
ENST00000639690.1:c.417A>C ENSP00000491917.1:n.417A>C
ENST00000639820.1:c.*574A>C ENSP00000491802.1:n.*574A>C
ENST00000639945.1:c.317A>C ENSP00000492866.1:p.Lys106Thr
ENST00000639981.1:c.223A>C
ENST00000640024.1:c.317A>C ENSP00000491238.1:p.Lys106Thr
ENST00000640222.1:c.238A>C
ENST00000640295.1:c.504A>C ENSP00000491027.1:n.504A>C
ENST00000640314.1:c.480A>C ENSP00000491315.1:n.480A>C
ENST00000640315.1:c.293A>C ENSP00000492089.1:p.Lys98Thr
ENST00000640322.1:c.233A>C ENSP00000491564.1:p.Lys78Thr
ENST00000640378.1:c.50A>C ENSP00000492030.1:p.Lys17Thr
ENST00000640418.1:c.374A>C ENSP00000492098.1:p.Lys125Thr
ENST00000640425.1:c.300A>C
ENST00000640572.1:c.300A>C
ENST00000640594.1:c.*360A>C ENSP00000491356.1:n.*360A>C
ENST00000640763.1:c.36A>C
ENST00000640835.1:c.199A>C
ENST00000640849.1:c.212A>C ENSP00000491701.1:p.Lys71Thr
ENST00000640903.1:c.403A>C
ENST00000640982.1:c.233A>C ENSP00000492299.1:p.Lys78Thr
ENST00000640992.1:c.233A>C ENSP00000492753.1:p.Lys78Thr
ENST00000306262.9:c.317A>C ENSP00000306247.5:p.Lys106Thr
ENST00000377332.7:c.317A>C ENSP00000366549.3:p.Lys106Thr
ENST00000393805.5:c.233A>C ENSP00000377394.1:p.Lys78Thr
ENST00000393808.7:c.248A>C ENSP00000377397.3:p.Lys83Thr
ENST00000433665.5:c.*360A>C ENSP00000408635.1:n.*360A>C
ENST00000455892.1:c.233A>C ENSP00000401375.1:p.Lys78Thr
ENST00000461199.5:n.322A>C
ENST00000461892.5:n.320A>C
ENST00000473122.5:n.289A>C
ENST00000484728.5:n.323A>C
NM_001042437.1:c.248A>C NP_001035902.1:p.Lys83Thr
NM_003896.3:c.317A>C NP_003887.3:p.Lys106Thr
XM_005264630.3:c.317A>C XP_005264687.1:p.Lys106Thr
XM_011533143.1:c.-245A>C XP_011531445.1:n.-245A>C
XR_939734.1:n.402A>C
XR_939735.1:n.402A>C
XR_939736.1:n.402A>C
NM_001354223.1:c.-245A>C NP_001341152.1:n.-245A>C
NM_001354224.1:c.-308A>C NP_001341153.1:n.-308A>C
NM_001354226.1:c.-245A>C NP_001341155.1:n.-245A>C
NM_001354227.1:c.233A>C NP_001341156.1:p.Lys78Thr
NM_001354229.1:c.233A>C NP_001341158.1:p.Lys78Thr
NM_001354233.1:c.-685A>C NP_001341162.1:n.-685A>C
NM_001354234.1:c.-649A>C NP_001341163.1:n.-649A>C
NM_001354238.1:c.233A>C NP_001341167.1:p.Lys78Thr
NM_001363847.1:c.317A>C NP_001350776.1:p.Lys106Thr
XM_017005202.2:c.233A>C XP_016860691.1:p.Lys78Thr
XM_017005203.2:c.-748A>C XP_016860692.1:n.-748A>C
XM_017005204.2:c.-748A>C XP_016860693.1:n.-748A>C
XM_017005205.2:c.-740A>C XP_016860694.1:n.-740A>C
XM_017005206.2:c.-649A>C XP_016860695.1:n.-649A>C
XM_017005208.2:c.-649A>C XP_016860697.1:n.-649A>C
XM_017005209.1:c.-300A>C XP_016860698.1:n.-300A>C
XM_017005212.2:c.-209A>C XP_016860701.1:n.-209A>C
XM_017005214.2:c.-245A>C XP_016860703.1:n.-245A>C
XR_001739019.1:n.402A>C
XR_001739020.1:n.402A>C
XR_001739021.1:n.402A>C
NM_003896.4:c.317A>C MANE Select NP_003887.3:p.Lys106Thr
NM_001042437.2:c.248A>C NP_001035902.1:p.Lys83Thr
NM_001354223.2:c.-245A>C NP_001341152.1:n.-245A>C
NM_001354224.2:c.-308A>C NP_001341153.1:n.-308A>C
NM_001354226.2:c.-245A>C NP_001341155.1:n.-245A>C
NM_001354227.2:c.233A>C NP_001341156.1:p.Lys78Thr
NM_001354229.2:c.233A>C NP_001341158.1:p.Lys78Thr
NM_001354233.2:c.-685A>C NP_001341162.1:n.-685A>C