Canonical Allele Identifier: CA25249333

Gene: ST6GALNAC3

Linked Data

• dbSNP Id: rs187201147
• gnomAD v3: 1-76226867-C-T
• gnomAD v4: 1-76226867-C-T
• MyVariant Identifiers: chr1:g.76692552C>T (hg19) ; chr1:g.76226867C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.76226867C>T , CM000663.2:g.76226867C>T	GRCh38
NC_000001.10:g.76692552C>T , CM000663.1:g.76692552C>T	GRCh37
NC_000001.9:g.76465140C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328299.4:c.19-86938C>T MANE Select	ENSP00000329214.3:n.19-86938C>T
ENST00000328299.3:c.19-86938C>T	ENSP00000329214.3:n.19-86938C>T
NM_001160011.1:c.19-86938C>T	NP_001153483.1:n.19-86938C>T
NM_152996.2:c.19-86938C>T	NP_694541.2:n.19-86938C>T
XM_006710553.2:c.-53-82639C>T	XP_006710616.1:n.-53-82639C>T
NM_001160011.2:c.19-86938C>T	NP_001153483.1:n.19-86938C>T
NM_001349105.1:c.18+151983C>T	NP_001336034.1:n.18+151983C>T
NM_001349106.1:c.-485-82639C>T	NP_001336035.1:n.-485-82639C>T
NM_001349107.1:c.19-86938C>T	NP_001336036.1:n.19-86938C>T
NM_001349108.1:c.18+151983C>T	NP_001336037.1:n.18+151983C>T
NM_001349109.1:c.19-86938C>T	NP_001336038.1:n.19-86938C>T
NM_001349110.1:c.19-86938C>T	NP_001336039.1:n.19-86938C>T
NM_001349111.1:c.-53-82639C>T	NP_001336040.1:n.-53-82639C>T
NM_152996.3:c.19-86938C>T	NP_694541.2:n.19-86938C>T
NR_146056.1:n.202-86938C>T
XR_001737094.2:n.152-86938C>T
NM_152996.4:c.19-86938C>T MANE Select	NP_694541.2:n.19-86938C>T
NM_001160011.3:c.19-86938C>T	NP_001153483.1:n.19-86938C>T
NM_001349105.2:c.18+151983C>T	NP_001336034.1:n.18+151983C>T
NM_001349106.2:c.-485-82639C>T	NP_001336035.1:n.-485-82639C>T
NM_001349107.2:c.19-86938C>T	NP_001336036.1:n.19-86938C>T
NM_001349108.2:c.18+151983C>T	NP_001336037.1:n.18+151983C>T
NM_001349109.2:c.19-86938C>T	NP_001336038.1:n.19-86938C>T
NM_001349110.2:c.19-86938C>T	NP_001336039.1:n.19-86938C>T
NM_001349111.2:c.-53-82639C>T	NP_001336040.1:n.-53-82639C>T
NR_146056.2:n.140-86938C>T
NM_001349109.3:c.19-86938C>T	NP_001336038.1:n.19-86938C>T