Canonical Allele Identifier: CA1176919641

Gene: ST6GALNAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.76226926T= , CM000663.2:g.76226926T=	GRCh38
NC_000001.10:g.76692611T= , CM000663.1:g.76692611T=	GRCh37
NC_000001.9:g.76465199T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328299.4:c.19-86879T= MANE Select	ENSP00000329214.3:n.19-86879T=
ENST00000328299.3:c.19-86879T=	ENSP00000329214.3:n.19-86879T=
NM_001160011.1:c.19-86879T=	NP_001153483.1:n.19-86879T=
NM_152996.2:c.19-86879T=	NP_694541.2:n.19-86879T=
XM_006710553.2:c.-53-82580T=	XP_006710616.1:n.-53-82580T=
NM_001160011.2:c.19-86879T=	NP_001153483.1:n.19-86879T=
NM_001349105.1:c.18+152042T=	NP_001336034.1:n.18+152042T=
NM_001349106.1:c.-485-82580T=	NP_001336035.1:n.-485-82580T=
NM_001349107.1:c.19-86879T=	NP_001336036.1:n.19-86879T=
NM_001349108.1:c.18+152042T=	NP_001336037.1:n.18+152042T=
NM_001349109.1:c.19-86879T=	NP_001336038.1:n.19-86879T=
NM_001349110.1:c.19-86879T=	NP_001336039.1:n.19-86879T=
NM_001349111.1:c.-53-82580T=	NP_001336040.1:n.-53-82580T=
NM_152996.3:c.19-86879T=	NP_694541.2:n.19-86879T=
NR_146056.1:n.202-86879T=
XR_001737094.2:n.152-86879T=
NM_152996.4:c.19-86879T= MANE Select	NP_694541.2:n.19-86879T=
NM_001160011.3:c.19-86879T=	NP_001153483.1:n.19-86879T=
NM_001349105.2:c.18+152042T=	NP_001336034.1:n.18+152042T=
NM_001349106.2:c.-485-82580T=	NP_001336035.1:n.-485-82580T=
NM_001349107.2:c.19-86879T=	NP_001336036.1:n.19-86879T=
NM_001349108.2:c.18+152042T=	NP_001336037.1:n.18+152042T=
NM_001349109.2:c.19-86879T=	NP_001336038.1:n.19-86879T=
NM_001349110.2:c.19-86879T=	NP_001336039.1:n.19-86879T=
NM_001349111.2:c.-53-82580T=	NP_001336040.1:n.-53-82580T=
NR_146056.2:n.140-86879T=
NM_001349109.3:c.19-86879T=	NP_001336038.1:n.19-86879T=