Canonical Allele Identifier: CA1977847690
Gene: B3GAT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62616594_62616604delinsGTGGAATCAAA , CM000673.2:g.62616594_62616604delinsGTGGAATCAAA GRCh38
NC_000011.9:g.62384066_62384076delinsGTGGAATCAAA , CM000673.1:g.62384066_62384076delinsGTGGAATCAAA GRCh37
NC_000011.8:g.62140642_62140652delinsGTGGAATCAAA NCBI36
NG_009845.1:g.8854_8864delinsGTGGAATCAAA
NG_031863.1:g.10572_10582delinsTTTGATTCCAC

Transcript Alleles

HGVS Amino-acid change
ENST00000265471.10:c.811_821delinsTTTGATTCCAC MANE Select ENSP00000265471.5:p.Phe271=
ENST00000265471.9:c.811_821delinsTTTGATTCCAC ENSP00000265471.5:p.Phe271=
ENST00000531383.5:c.811_821delinsTTTGATTCCAC ENSP00000431359.1:p.Phe271=
ENST00000532585.5:c.*933_*943delinsTTTGATTCCAC ENSP00000432604.1:n.*933_*943delinsTTTGATTCCAC
ENST00000534026.5:c.811_821delinsTTTGATTCCAC ENSP00000432474.1:p.Phe271=
NM_001288721.1:c.790_800delinsTTTGATTCCAC NP_001275650.1:p.Phe264=
NM_001288722.1:c.811_821delinsTTTGATTCCAC NP_001275651.1:p.Phe271=
NM_001288723.1:c.811_821delinsTTTGATTCCAC NP_001275652.1:p.Phe271=
NM_012200.3:c.811_821delinsTTTGATTCCAC NP_036332.2:p.Phe271=
NR_109991.1:n.1029_1039delinsTTTGATTCCAC
XM_011544936.1:c.790_800delinsTTTGATTCCAC XP_011543238.1:p.Phe264=
NM_012200.4:c.811_821delinsTTTGATTCCAC MANE Select NP_036332.2:p.Phe271=
NM_001288721.2:c.790_800delinsTTTGATTCCAC NP_001275650.1:p.Phe264=
NM_001288722.2:c.811_821delinsTTTGATTCCAC NP_001275651.1:p.Phe271=
NM_001288723.2:c.811_821delinsTTTGATTCCAC NP_001275652.1:p.Phe271=
NR_109991.2:n.840_850delinsTTTGATTCCAC