Canonical Allele Identifier: CA427138610

Gene: ST3GAL5

Linked Data

• MyVariant Identifiers: chr2:g.86088310A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85861187A>G , CM000664.2:g.85861187A>G	GRCh38
NC_000002.11:g.86088310A>G , CM000664.1:g.86088310A>G	GRCh37
NC_000002.10:g.85941821A>G	NCBI36
NG_012807.1:g.32848T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306262.10:c.*56T>C	ENSP00000306247.6:n.*56T>C
ENST00000377332.8:c.312T>C	ENSP00000366549.4:p.His104=
ENST00000393805.6:c.228T>C	ENSP00000377394.1:p.His76=
ENST00000393808.8:c.243T>C	ENSP00000377397.3:p.His81=
ENST00000433665.6:c.*355T>C	ENSP00000408635.1:n.*355T>C
ENST00000461199.6:n.764T>C
ENST00000461892.6:n.317T>C
ENST00000473122.6:c.312T>C	ENSP00000491314.1:p.His104=
ENST00000484728.6:n.323T>C
ENST00000638178.1:c.228T>C	ENSP00000492103.1:p.His76=
ENST00000638227.1:c.*355T>C	ENSP00000492602.1:n.*355T>C
ENST00000638288.1:c.228T>C	ENSP00000491699.1:p.His76=
ENST00000638321.1:c.209T>C
ENST00000638484.1:c.*355T>C	ENSP00000492635.1:n.*355T>C
ENST00000638523.1:c.209T>C
ENST00000638542.1:c.206+2175T>C	ENSP00000492468.1:n.206+2175T>C
ENST00000638572.2:c.312T>C MANE Select	ENSP00000491316.1:p.His104=
ENST00000638581.1:n.338T>C
ENST00000638659.1:c.498T>C
ENST00000638678.1:c.310T>C
ENST00000638855.1:c.206+2175T>C	ENSP00000490979.1:n.206+2175T>C
ENST00000638885.1:c.312T>C	ENSP00000492209.1:p.His104=
ENST00000638956.1:c.312T>C	ENSP00000492097.1:p.His104=
ENST00000638986.1:c.228T>C	ENSP00000491853.1:p.His76=
ENST00000639119.1:c.312T>C	ENSP00000492045.1:p.His104=
ENST00000639184.1:c.228T>C	ENSP00000492305.1:p.His76=
ENST00000639202.1:c.195T>C	ENSP00000492710.1:p.His65=
ENST00000639216.1:n.334T>C
ENST00000639305.1:c.310T>C
ENST00000639311.1:c.312T>C	ENSP00000491398.1:p.His104=
ENST00000639421.1:c.499T>C	ENSP00000491029.1:n.499T>C
ENST00000639432.1:c.228T>C	ENSP00000491828.1:p.His76=
ENST00000639519.1:c.114T>C	ENSP00000491857.1:p.His38=
ENST00000639541.1:c.312T>C	ENSP00000492280.1:p.His104=
ENST00000639608.1:c.312T>C	ENSP00000492473.1:p.His104=
ENST00000639690.1:c.412T>C	ENSP00000491917.1:n.412T>C
ENST00000639820.1:c.*569T>C	ENSP00000491802.1:n.*569T>C
ENST00000639945.1:c.312T>C	ENSP00000492866.1:p.His104=
ENST00000639981.1:c.218T>C
ENST00000640024.1:c.312T>C	ENSP00000491238.1:p.His104=
ENST00000640222.1:c.233T>C
ENST00000640295.1:c.499T>C	ENSP00000491027.1:n.499T>C
ENST00000640314.1:c.475T>C	ENSP00000491315.1:n.475T>C
ENST00000640315.1:c.288T>C	ENSP00000492089.1:p.His96=
ENST00000640322.1:c.228T>C	ENSP00000491564.1:p.His76=
ENST00000640378.1:c.45T>C	ENSP00000492030.1:p.His15=
ENST00000640418.1:c.369T>C	ENSP00000492098.1:p.His123=
ENST00000640425.1:c.295T>C
ENST00000640572.1:c.295T>C
ENST00000640594.1:c.*355T>C	ENSP00000491356.1:n.*355T>C
ENST00000640763.1:c.31T>C
ENST00000640835.1:c.194T>C
ENST00000640849.1:c.207T>C	ENSP00000491701.1:p.His69=
ENST00000640903.1:c.398T>C
ENST00000640982.1:c.228T>C	ENSP00000492299.1:p.His76=
ENST00000640992.1:c.228T>C	ENSP00000492753.1:p.His76=
ENST00000306262.9:c.312T>C	ENSP00000306247.5:p.His104=
ENST00000377332.7:c.312T>C	ENSP00000366549.3:p.His104=
ENST00000393805.5:c.228T>C	ENSP00000377394.1:p.His76=
ENST00000393808.7:c.243T>C	ENSP00000377397.3:p.His81=
ENST00000433665.5:c.*355T>C	ENSP00000408635.1:n.*355T>C
ENST00000455892.1:c.228T>C	ENSP00000401375.1:p.His76=
ENST00000461199.5:n.317T>C
ENST00000461892.5:n.315T>C
ENST00000473122.5:n.284T>C
ENST00000484728.5:n.318T>C
NM_001042437.1:c.243T>C	NP_001035902.1:p.His81=
NM_003896.3:c.312T>C	NP_003887.3:p.His104=
XM_005264630.3:c.312T>C	XP_005264687.1:p.His104=
XM_011533143.1:c.-250T>C	XP_011531445.1:n.-250T>C
XR_939734.1:n.397T>C
XR_939735.1:n.397T>C
XR_939736.1:n.397T>C
NM_001354223.1:c.-250T>C	NP_001341152.1:n.-250T>C
NM_001354224.1:c.-313T>C	NP_001341153.1:n.-313T>C
NM_001354226.1:c.-250T>C	NP_001341155.1:n.-250T>C
NM_001354227.1:c.228T>C	NP_001341156.1:p.His76=
NM_001354229.1:c.228T>C	NP_001341158.1:p.His76=
NM_001354233.1:c.-690T>C	NP_001341162.1:n.-690T>C
NM_001354234.1:c.-654T>C	NP_001341163.1:n.-654T>C
NM_001354238.1:c.228T>C	NP_001341167.1:p.His76=
NM_001363847.1:c.312T>C	NP_001350776.1:p.His104=
XM_017005202.2:c.228T>C	XP_016860691.1:p.His76=
XM_017005203.2:c.-753T>C	XP_016860692.1:n.-753T>C
XM_017005204.2:c.-753T>C	XP_016860693.1:n.-753T>C
XM_017005205.2:c.-745T>C	XP_016860694.1:n.-745T>C
XM_017005206.2:c.-654T>C	XP_016860695.1:n.-654T>C
XM_017005208.2:c.-654T>C	XP_016860697.1:n.-654T>C
XM_017005209.1:c.-305T>C	XP_016860698.1:n.-305T>C
XM_017005212.2:c.-214T>C	XP_016860701.1:n.-214T>C
XM_017005214.2:c.-250T>C	XP_016860703.1:n.-250T>C
XR_001739019.1:n.397T>C
XR_001739020.1:n.397T>C
XR_001739021.1:n.397T>C
NM_003896.4:c.312T>C MANE Select	NP_003887.3:p.His104=
NM_001042437.2:c.243T>C	NP_001035902.1:p.His81=
NM_001354223.2:c.-250T>C	NP_001341152.1:n.-250T>C
NM_001354224.2:c.-313T>C	NP_001341153.1:n.-313T>C
NM_001354226.2:c.-250T>C	NP_001341155.1:n.-250T>C
NM_001354227.2:c.228T>C	NP_001341156.1:p.His76=
NM_001354229.2:c.228T>C	NP_001341158.1:p.His76=
NM_001354233.2:c.-690T>C	NP_001341162.1:n.-690T>C