Canonical Allele Identifier: CA347533945

Gene: ST3GAL5

Linked Data

• MyVariant Identifiers: chr2:g.86088319G>C (hg19) ; chr2:g.85861196G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85861196G>C , CM000664.2:g.85861196G>C	GRCh38
NC_000002.11:g.86088319G>C , CM000664.1:g.86088319G>C	GRCh37
NC_000002.10:g.85941830G>C	NCBI36
NG_012807.1:g.32839C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306262.10:c.*47C>G	ENSP00000306247.6:n.*47C>G
ENST00000377332.8:c.303C>G	ENSP00000366549.4:p.Asp101Glu
ENST00000393805.6:c.219C>G	ENSP00000377394.1:p.Asp73Glu
ENST00000393808.8:c.234C>G	ENSP00000377397.3:p.Asp78Glu
ENST00000433665.6:c.*346C>G	ENSP00000408635.1:n.*346C>G
ENST00000461199.6:n.755C>G
ENST00000461892.6:n.308C>G
ENST00000473122.6:c.303C>G	ENSP00000491314.1:p.Asp101Glu
ENST00000484728.6:n.314C>G
ENST00000638178.1:c.219C>G	ENSP00000492103.1:p.Asp73Glu
ENST00000638227.1:c.*346C>G	ENSP00000492602.1:n.*346C>G
ENST00000638288.1:c.219C>G	ENSP00000491699.1:p.Asp73Glu
ENST00000638321.1:c.200C>G
ENST00000638484.1:c.*346C>G	ENSP00000492635.1:n.*346C>G
ENST00000638523.1:c.200C>G
ENST00000638542.1:c.206+2166C>G	ENSP00000492468.1:n.206+2166C>G
ENST00000638572.2:c.303C>G MANE Select	ENSP00000491316.1:p.Asp101Glu
ENST00000638581.1:n.329C>G
ENST00000638659.1:c.489C>G
ENST00000638678.1:c.301C>G
ENST00000638855.1:c.206+2166C>G	ENSP00000490979.1:n.206+2166C>G
ENST00000638885.1:c.303C>G	ENSP00000492209.1:p.Asp101Glu
ENST00000638956.1:c.303C>G	ENSP00000492097.1:p.Asp101Glu
ENST00000638986.1:c.219C>G	ENSP00000491853.1:p.Asp73Glu
ENST00000639119.1:c.303C>G	ENSP00000492045.1:p.Asp101Glu
ENST00000639184.1:c.219C>G	ENSP00000492305.1:p.Asp73Glu
ENST00000639202.1:c.186C>G	ENSP00000492710.1:p.Asp62Glu
ENST00000639216.1:n.325C>G
ENST00000639305.1:c.301C>G
ENST00000639311.1:c.303C>G	ENSP00000491398.1:p.Asp101Glu
ENST00000639421.1:c.490C>G	ENSP00000491029.1:n.490C>G
ENST00000639432.1:c.219C>G	ENSP00000491828.1:p.Asp73Glu
ENST00000639519.1:c.105C>G	ENSP00000491857.1:p.Asp35Glu
ENST00000639541.1:c.303C>G	ENSP00000492280.1:p.Asp101Glu
ENST00000639608.1:c.303C>G	ENSP00000492473.1:p.Asp101Glu
ENST00000639690.1:c.403C>G	ENSP00000491917.1:n.403C>G
ENST00000639820.1:c.*560C>G	ENSP00000491802.1:n.*560C>G
ENST00000639945.1:c.303C>G	ENSP00000492866.1:p.Asp101Glu
ENST00000639981.1:c.209C>G
ENST00000640024.1:c.303C>G	ENSP00000491238.1:p.Asp101Glu
ENST00000640222.1:c.224C>G
ENST00000640295.1:c.490C>G	ENSP00000491027.1:n.490C>G
ENST00000640314.1:c.466C>G	ENSP00000491315.1:n.466C>G
ENST00000640315.1:c.279C>G	ENSP00000492089.1:p.Asp93Glu
ENST00000640322.1:c.219C>G	ENSP00000491564.1:p.Asp73Glu
ENST00000640378.1:c.36C>G	ENSP00000492030.1:p.Asp12Glu
ENST00000640418.1:c.360C>G	ENSP00000492098.1:p.Asp120Glu
ENST00000640425.1:c.286C>G
ENST00000640572.1:c.286C>G
ENST00000640594.1:c.*346C>G	ENSP00000491356.1:n.*346C>G
ENST00000640763.1:c.22C>G
ENST00000640835.1:c.185C>G
ENST00000640849.1:c.198C>G	ENSP00000491701.1:p.Asp66Glu
ENST00000640903.1:c.389C>G
ENST00000640982.1:c.219C>G	ENSP00000492299.1:p.Asp73Glu
ENST00000640992.1:c.219C>G	ENSP00000492753.1:p.Asp73Glu
ENST00000306262.9:c.303C>G	ENSP00000306247.5:p.Asp101Glu
ENST00000377332.7:c.303C>G	ENSP00000366549.3:p.Asp101Glu
ENST00000393805.5:c.219C>G	ENSP00000377394.1:p.Asp73Glu
ENST00000393808.7:c.234C>G	ENSP00000377397.3:p.Asp78Glu
ENST00000433665.5:c.*346C>G	ENSP00000408635.1:n.*346C>G
ENST00000455892.1:c.219C>G	ENSP00000401375.1:p.Asp73Glu
ENST00000461199.5:n.308C>G
ENST00000461892.5:n.306C>G
ENST00000473122.5:n.275C>G
ENST00000484728.5:n.309C>G
NM_001042437.1:c.234C>G	NP_001035902.1:p.Asp78Glu
NM_003896.3:c.303C>G	NP_003887.3:p.Asp101Glu
XM_005264630.3:c.303C>G	XP_005264687.1:p.Asp101Glu
XM_011533143.1:c.-259C>G	XP_011531445.1:n.-259C>G
XR_939734.1:n.388C>G
XR_939735.1:n.388C>G
XR_939736.1:n.388C>G
NM_001354223.1:c.-259C>G	NP_001341152.1:n.-259C>G
NM_001354224.1:c.-322C>G	NP_001341153.1:n.-322C>G
NM_001354226.1:c.-259C>G	NP_001341155.1:n.-259C>G
NM_001354227.1:c.219C>G	NP_001341156.1:p.Asp73Glu
NM_001354229.1:c.219C>G	NP_001341158.1:p.Asp73Glu
NM_001354233.1:c.-699C>G	NP_001341162.1:n.-699C>G
NM_001354234.1:c.-663C>G	NP_001341163.1:n.-663C>G
NM_001354238.1:c.219C>G	NP_001341167.1:p.Asp73Glu
NM_001363847.1:c.303C>G	NP_001350776.1:p.Asp101Glu
XM_017005202.2:c.219C>G	XP_016860691.1:p.Asp73Glu
XM_017005203.2:c.-762C>G	XP_016860692.1:n.-762C>G
XM_017005204.2:c.-762C>G	XP_016860693.1:n.-762C>G
XM_017005205.2:c.-754C>G	XP_016860694.1:n.-754C>G
XM_017005206.2:c.-663C>G	XP_016860695.1:n.-663C>G
XM_017005208.2:c.-663C>G	XP_016860697.1:n.-663C>G
XM_017005209.1:c.-314C>G	XP_016860698.1:n.-314C>G
XM_017005212.2:c.-223C>G	XP_016860701.1:n.-223C>G
XM_017005214.2:c.-259C>G	XP_016860703.1:n.-259C>G
XR_001739019.1:n.388C>G
XR_001739020.1:n.388C>G
XR_001739021.1:n.388C>G
NM_003896.4:c.303C>G MANE Select	NP_003887.3:p.Asp101Glu
NM_001042437.2:c.234C>G	NP_001035902.1:p.Asp78Glu
NM_001354223.2:c.-259C>G	NP_001341152.1:n.-259C>G
NM_001354224.2:c.-322C>G	NP_001341153.1:n.-322C>G
NM_001354226.2:c.-259C>G	NP_001341155.1:n.-259C>G
NM_001354227.2:c.219C>G	NP_001341156.1:p.Asp73Glu
NM_001354229.2:c.219C>G	NP_001341158.1:p.Asp73Glu
NM_001354233.2:c.-699C>G	NP_001341162.1:n.-699C>G