Canonical Allele Identifier: CA915098

Gene: ST6GALNAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.76412234C>T , CM000663.2:g.76412234C>T	GRCh38
NC_000001.10:g.76877919C>T , CM000663.1:g.76877919C>T	GRCh37
NC_000001.9:g.76650507C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_152996.4:c.440C>T MANE Select	NP_694541.2:p.Ala147Val
ENST00000328299.4:c.440C>T MANE Select	ENSP00000329214.3:p.Ala147Val
NM_001160011.1:c.440C>T	NP_001153483.1:p.Ala147Val
NM_001160011.2:c.440C>T	NP_001153483.1:p.Ala147Val
NM_001160011.3:c.440C>T	NP_001153483.1:p.Ala147Val
NM_001349105.1:c.245C>T	NP_001336034.1:p.Ala82Val
NM_001349105.2:c.245C>T	NP_001336034.1:p.Ala82Val
NM_001349106.1:c.176C>T	NP_001336035.1:p.Ala59Val
NM_001349106.2:c.176C>T	NP_001336035.1:p.Ala59Val
NM_001349107.1:c.440C>T	NP_001336036.1:p.Ala147Val
NM_001349107.2:c.440C>T	NP_001336036.1:p.Ala147Val
NM_001349108.1:c.245C>T	NP_001336037.1:p.Ala82Val
NM_001349108.2:c.245C>T	NP_001336037.1:p.Ala82Val
NM_001349109.1:c.440C>T	NP_001336038.1:p.Ala147Val
NM_001349109.2:c.440C>T	NP_001336038.1:p.Ala147Val
NM_001349109.3:c.440C>T	NP_001336038.1:p.Ala147Val
NM_001349110.1:c.440C>T	NP_001336039.1:p.Ala147Val
NM_001349110.2:c.440C>T	NP_001336039.1:p.Ala147Val
NM_001349111.1:c.476C>T	NP_001336040.1:p.Ala159Val
NM_001349111.2:c.476C>T	NP_001336040.1:p.Ala159Val
NM_152996.2:c.440C>T	NP_694541.2:p.Ala147Val
NM_152996.3:c.440C>T	NP_694541.2:p.Ala147Val
NR_146056.1:n.623C>T
NR_146056.2:n.561C>T
ENST00000328299.3:c.440C>T	ENSP00000329214.3:p.Ala147Val
ENST00000464140.1:n.314C>T
ENST00000621530.1:c.227C>T	ENSP00000480283.1:p.Ala76Val
XM_006710553.2:c.476C>T	XP_006710616.1:p.Ala159Val
XM_017000937.2:c.494C>T	XP_016856426.1:p.Ala165Val
XM_017000938.1:c.494C>T	XP_016856427.1:p.Ala165Val
XM_017000939.1:c.494C>T	XP_016856428.1:p.Ala165Val
XM_017000941.2:c.176C>T	XP_016856430.1:p.Ala59Val
XM_017000942.2:c.176C>T	XP_016856431.1:p.Ala59Val
XR_001737094.2:n.573C>T