Canonical Allele Identifier: CA1176951828
Gene: ST6GALNAC3 HGNC NCBI

Linked Data

dbSNP Id: rs10873876

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.76306643T>G , CM000663.2:g.76306643T>G GRCh38
NC_000001.10:g.76772328T>G , CM000663.1:g.76772328T>G GRCh37
NC_000001.9:g.76544916T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000328299.4:c.19-7162T>G MANE Select ENSP00000329214.3:n.19-7162T>G
ENST00000328299.3:c.19-7162T>G ENSP00000329214.3:n.19-7162T>G
NM_001160011.1:c.19-7162T>G NP_001153483.1:n.19-7162T>G
NM_152996.2:c.19-7162T>G NP_694541.2:n.19-7162T>G
XM_006710553.2:c.-53-2863T>G XP_006710616.1:n.-53-2863T>G
NM_001160011.2:c.19-7162T>G NP_001153483.1:n.19-7162T>G
NM_001349105.1:c.19-105365T>G NP_001336034.1:n.19-105365T>G
NM_001349106.1:c.-485-2863T>G NP_001336035.1:n.-485-2863T>G
NM_001349107.1:c.19-7162T>G NP_001336036.1:n.19-7162T>G
NM_001349108.1:c.19-105365T>G NP_001336037.1:n.19-105365T>G
NM_001349109.1:c.19-7162T>G NP_001336038.1:n.19-7162T>G
NM_001349110.1:c.19-7162T>G NP_001336039.1:n.19-7162T>G
NM_001349111.1:c.-53-2863T>G NP_001336040.1:n.-53-2863T>G
NM_152996.3:c.19-7162T>G NP_694541.2:n.19-7162T>G
NR_146056.1:n.202-7162T>G
XM_017000937.2:c.73-7162T>G XP_016856426.1:n.73-7162T>G
XM_017000938.1:c.73-7162T>G XP_016856427.1:n.73-7162T>G
XM_017000939.1:c.73-7162T>G XP_016856428.1:n.73-7162T>G
XM_017000941.2:c.-246-7162T>G XP_016856430.1:n.-246-7162T>G
XM_017000942.2:c.-246-7162T>G XP_016856431.1:n.-246-7162T>G
XR_001737094.2:n.152-7162T>G
NM_152996.4:c.19-7162T>G MANE Select NP_694541.2:n.19-7162T>G
NM_001160011.3:c.19-7162T>G NP_001153483.1:n.19-7162T>G
NM_001349105.2:c.19-105365T>G NP_001336034.1:n.19-105365T>G
NM_001349106.2:c.-485-2863T>G NP_001336035.1:n.-485-2863T>G
NM_001349107.2:c.19-7162T>G NP_001336036.1:n.19-7162T>G
NM_001349108.2:c.19-105365T>G NP_001336037.1:n.19-105365T>G
NM_001349109.2:c.19-7162T>G NP_001336038.1:n.19-7162T>G
NM_001349110.2:c.19-7162T>G NP_001336039.1:n.19-7162T>G
NM_001349111.2:c.-53-2863T>G NP_001336040.1:n.-53-2863T>G
NR_146056.2:n.140-7162T>G
NM_001349109.3:c.19-7162T>G NP_001336038.1:n.19-7162T>G