Canonical Allele Identifier: CA427138611
Gene: ST3GAL5 HGNC NCBI

Linked Data

dbSNP Id: rs1399904609
gnomAD v2: 2-86088313-G-A
gnomAD v3: 2-85861190-G-A
gnomAD v4: 2-85861190-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85861190G>A , CM000664.2:g.85861190G>A GRCh38
NC_000002.11:g.86088313G>A , CM000664.1:g.86088313G>A GRCh37
NC_000002.10:g.85941824G>A NCBI36
NG_012807.1:g.32845C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306262.10:c.*53C>T ENSP00000306247.6:n.*53C>T
ENST00000377332.8:c.309C>T ENSP00000366549.4:p.Asp103=
ENST00000393805.6:c.225C>T ENSP00000377394.1:p.Asp75=
ENST00000393808.8:c.240C>T ENSP00000377397.3:p.Asp80=
ENST00000433665.6:c.*352C>T ENSP00000408635.1:n.*352C>T
ENST00000461199.6:n.761C>T
ENST00000461892.6:n.314C>T
ENST00000473122.6:c.309C>T ENSP00000491314.1:p.Asp103=
ENST00000484728.6:n.320C>T
ENST00000638178.1:c.225C>T ENSP00000492103.1:p.Asp75=
ENST00000638227.1:c.*352C>T ENSP00000492602.1:n.*352C>T
ENST00000638288.1:c.225C>T ENSP00000491699.1:p.Asp75=
ENST00000638321.1:c.206C>T
ENST00000638484.1:c.*352C>T ENSP00000492635.1:n.*352C>T
ENST00000638523.1:c.206C>T
ENST00000638542.1:c.206+2172C>T ENSP00000492468.1:n.206+2172C>T
ENST00000638572.2:c.309C>T MANE Select ENSP00000491316.1:p.Asp103=
ENST00000638581.1:n.335C>T
ENST00000638659.1:c.495C>T
ENST00000638678.1:c.307C>T
ENST00000638855.1:c.206+2172C>T ENSP00000490979.1:n.206+2172C>T
ENST00000638885.1:c.309C>T ENSP00000492209.1:p.Asp103=
ENST00000638956.1:c.309C>T ENSP00000492097.1:p.Asp103=
ENST00000638986.1:c.225C>T ENSP00000491853.1:p.Asp75=
ENST00000639119.1:c.309C>T ENSP00000492045.1:p.Asp103=
ENST00000639184.1:c.225C>T ENSP00000492305.1:p.Asp75=
ENST00000639202.1:c.192C>T ENSP00000492710.1:p.Asp64=
ENST00000639216.1:n.331C>T
ENST00000639305.1:c.307C>T
ENST00000639311.1:c.309C>T ENSP00000491398.1:p.Asp103=
ENST00000639421.1:c.496C>T ENSP00000491029.1:n.496C>T
ENST00000639432.1:c.225C>T ENSP00000491828.1:p.Asp75=
ENST00000639519.1:c.111C>T ENSP00000491857.1:p.Asp37=
ENST00000639541.1:c.309C>T ENSP00000492280.1:p.Asp103=
ENST00000639608.1:c.309C>T ENSP00000492473.1:p.Asp103=
ENST00000639690.1:c.409C>T ENSP00000491917.1:n.409C>T
ENST00000639820.1:c.*566C>T ENSP00000491802.1:n.*566C>T
ENST00000639945.1:c.309C>T ENSP00000492866.1:p.Asp103=
ENST00000639981.1:c.215C>T
ENST00000640024.1:c.309C>T ENSP00000491238.1:p.Asp103=
ENST00000640222.1:c.230C>T
ENST00000640295.1:c.496C>T ENSP00000491027.1:n.496C>T
ENST00000640314.1:c.472C>T ENSP00000491315.1:n.472C>T
ENST00000640315.1:c.285C>T ENSP00000492089.1:p.Asp95=
ENST00000640322.1:c.225C>T ENSP00000491564.1:p.Asp75=
ENST00000640378.1:c.42C>T ENSP00000492030.1:p.Asp14=
ENST00000640418.1:c.366C>T ENSP00000492098.1:p.Asp122=
ENST00000640425.1:c.292C>T
ENST00000640572.1:c.292C>T
ENST00000640594.1:c.*352C>T ENSP00000491356.1:n.*352C>T
ENST00000640763.1:c.28C>T
ENST00000640835.1:c.191C>T
ENST00000640849.1:c.204C>T ENSP00000491701.1:p.Asp68=
ENST00000640903.1:c.395C>T
ENST00000640982.1:c.225C>T ENSP00000492299.1:p.Asp75=
ENST00000640992.1:c.225C>T ENSP00000492753.1:p.Asp75=
ENST00000306262.9:c.309C>T ENSP00000306247.5:p.Asp103=
ENST00000377332.7:c.309C>T ENSP00000366549.3:p.Asp103=
ENST00000393805.5:c.225C>T ENSP00000377394.1:p.Asp75=
ENST00000393808.7:c.240C>T ENSP00000377397.3:p.Asp80=
ENST00000433665.5:c.*352C>T ENSP00000408635.1:n.*352C>T
ENST00000455892.1:c.225C>T ENSP00000401375.1:p.Asp75=
ENST00000461199.5:n.314C>T
ENST00000461892.5:n.312C>T
ENST00000473122.5:n.281C>T
ENST00000484728.5:n.315C>T
NM_001042437.1:c.240C>T NP_001035902.1:p.Asp80=
NM_003896.3:c.309C>T NP_003887.3:p.Asp103=
XM_005264630.3:c.309C>T XP_005264687.1:p.Asp103=
XM_011533143.1:c.-253C>T XP_011531445.1:n.-253C>T
XR_939734.1:n.394C>T
XR_939735.1:n.394C>T
XR_939736.1:n.394C>T
NM_001354223.1:c.-253C>T NP_001341152.1:n.-253C>T
NM_001354224.1:c.-316C>T NP_001341153.1:n.-316C>T
NM_001354226.1:c.-253C>T NP_001341155.1:n.-253C>T
NM_001354227.1:c.225C>T NP_001341156.1:p.Asp75=
NM_001354229.1:c.225C>T NP_001341158.1:p.Asp75=
NM_001354233.1:c.-693C>T NP_001341162.1:n.-693C>T
NM_001354234.1:c.-657C>T NP_001341163.1:n.-657C>T
NM_001354238.1:c.225C>T NP_001341167.1:p.Asp75=
NM_001363847.1:c.309C>T NP_001350776.1:p.Asp103=
XM_017005202.2:c.225C>T XP_016860691.1:p.Asp75=
XM_017005203.2:c.-756C>T XP_016860692.1:n.-756C>T
XM_017005204.2:c.-756C>T XP_016860693.1:n.-756C>T
XM_017005205.2:c.-748C>T XP_016860694.1:n.-748C>T
XM_017005206.2:c.-657C>T XP_016860695.1:n.-657C>T
XM_017005208.2:c.-657C>T XP_016860697.1:n.-657C>T
XM_017005209.1:c.-308C>T XP_016860698.1:n.-308C>T
XM_017005212.2:c.-217C>T XP_016860701.1:n.-217C>T
XM_017005214.2:c.-253C>T XP_016860703.1:n.-253C>T
XR_001739019.1:n.394C>T
XR_001739020.1:n.394C>T
XR_001739021.1:n.394C>T
NM_003896.4:c.309C>T MANE Select NP_003887.3:p.Asp103=
NM_001042437.2:c.240C>T NP_001035902.1:p.Asp80=
NM_001354223.2:c.-253C>T NP_001341152.1:n.-253C>T
NM_001354224.2:c.-316C>T NP_001341153.1:n.-316C>T
NM_001354226.2:c.-253C>T NP_001341155.1:n.-253C>T
NM_001354227.2:c.225C>T NP_001341156.1:p.Asp75=
NM_001354229.2:c.225C>T NP_001341158.1:p.Asp75=
NM_001354233.2:c.-693C>T NP_001341162.1:n.-693C>T