Canonical Allele Identifier: CA10924645
Gene: ST6GALNAC3 HGNC NCBI

Linked Data

dbSNP Id: rs527974

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.76226810G>A , CM000663.2:g.76226810G>A GRCh38
NC_000001.10:g.76692495G>A , CM000663.1:g.76692495G>A GRCh37
NC_000001.9:g.76465083G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000328299.4:c.19-86995G>A MANE Select ENSP00000329214.3:p.=
ENST00000328299.3:c.19-86995G>A ENSP00000329214.3:p.=
NM_001160011.1:c.19-86995G>A NP_001153483.1:p.=
NM_152996.2:c.19-86995G>A NP_694541.2:p.=
XM_006710553.2:c.-53-82696G>A XP_006710616.1:p.=
NM_001160011.2:c.19-86995G>A NP_001153483.1:p.=
NM_001349105.1:c.18+151926G>A NP_001336034.1:p.=
NM_001349106.1:c.-485-82696G>A NP_001336035.1:p.=
NM_001349107.1:c.19-86995G>A NP_001336036.1:p.=
NM_001349108.1:c.18+151926G>A NP_001336037.1:p.=
NM_001349109.1:c.19-86995G>A NP_001336038.1:p.=
NM_001349110.1:c.19-86995G>A NP_001336039.1:p.=
NM_001349111.1:c.-53-82696G>A NP_001336040.1:p.=
NM_152996.3:c.19-86995G>A NP_694541.2:p.=
NR_146056.1:n.202-86995G>A
XR_001737094.2:n.152-86995G>A
NM_152996.4:c.19-86995G>A MANE Select NP_694541.2:p.=
NM_001160011.3:c.19-86995G>A NP_001153483.1:p.=
NM_001349105.2:c.18+151926G>A NP_001336034.1:p.=
NM_001349106.2:c.-485-82696G>A NP_001336035.1:p.=
NM_001349107.2:c.19-86995G>A NP_001336036.1:p.=
NM_001349108.2:c.18+151926G>A NP_001336037.1:p.=
NM_001349109.2:c.19-86995G>A NP_001336038.1:p.=
NM_001349110.2:c.19-86995G>A NP_001336039.1:p.=
NM_001349111.2:c.-53-82696G>A NP_001336040.1:p.=
NR_146056.2:n.140-86995G>A
NM_001349109.3:c.19-86995G>A NP_001336038.1:p.=