Canonical Allele Identifier: CA1553917002
Gene: MARVELD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.69420174_69420196delinsTTGGATCACCACCATTATTATTC , CM000667.2:g.69420174_69420196delinsTTGGATCACCACCATTATTATTC GRCh38
NC_000005.9:g.68716001_68716023delinsTTGGATCACCACCATTATTATTC , CM000667.1:g.68716001_68716023delinsTTGGATCACCACCATTATTATTC GRCh37
NC_000005.8:g.68751757_68751779delinsTTGGATCACCACCATTATTATTC NCBI36
NG_017201.1:g.10063_10085delinsTTGGATCACCACCATTATTATTC
NG_017201.2:g.10063_10085delinsTTGGATCACCACCATTATTATTC

Transcript Alleles

HGVS Amino-acid change
ENST00000325631.10:c.789_811delinsTTGGATCACCACCATTATTATTC MANE Select ENSP00000323264.5:p.Ala263=
ENST00000413223.3:c.725+64_725+86delinsTTGGATCACCACCATTATTATTC ENSP00000398922.2:n.725+64_725+86delinsTTGGATCACCACCATTATTATT...
ENST00000436532.7:c.725+64_725+86delinsTTGGATCACCACCATTATTATTC ENSP00000414776.2:n.725+64_725+86delinsTTGGATCACCACCATTATTATT...
ENST00000645446.1:c.789_811delinsTTGGATCACCACCATTATTATTC ENSP00000494616.1:p.Ala263=
ENST00000647531.1:c.789_811delinsTTGGATCACCACCATTATTATTC ENSP00000493858.1:p.Ala263=
ENST00000325631.9:c.789_811delinsTTGGATCACCACCATTATTATTC ENSP00000323264.5:p.Ala263=
ENST00000413223.2:c.725+64_725+86delinsTTGGATCACCACCATTATTATTC ENSP00000398922.2:n.725+64_725+86delinsTTGGATCACCACCATTATTATT...
ENST00000436532.6:c.725+64_725+86delinsTTGGATCACCACCATTATTATTC ENSP00000414776.2:n.725+64_725+86delinsTTGGATCACCACCATTATTATT...
ENST00000454295.6:c.789_811delinsTTGGATCACCACCATTATTATTC ENSP00000396244.2:p.Ala263=
ENST00000512803.5:c.789_811delinsTTGGATCACCACCATTATTATTC ENSP00000423490.1:p.Ala263=
NM_001038603.2:c.789_811delinsTTGGATCACCACCATTATTATTC NP_001033692.2:p.Ala263=
NM_001244734.1:c.789_811delinsTTGGATCACCACCATTATTATTC NP_001231663.1:p.Ala263=
XM_005248445.3:c.789_811delinsTTGGATCACCACCATTATTATTC XP_005248502.1:p.Ala263=
XM_005248446.3:c.789_811delinsTTGGATCACCACCATTATTATTC XP_005248503.1:p.Ala263=
XM_005248447.3:c.789_811delinsTTGGATCACCACCATTATTATTC XP_005248504.1:p.Ala263=
XM_005248445.4:c.789_811delinsTTGGATCACCACCATTATTATTC XP_005248502.1:p.Ala263=
XM_005248446.4:c.789_811delinsTTGGATCACCACCATTATTATTC XP_005248503.1:p.Ala263=
XM_005248447.4:c.789_811delinsTTGGATCACCACCATTATTATTC XP_005248504.1:p.Ala263=
NM_001038603.3:c.789_811delinsTTGGATCACCACCATTATTATTC MANE Select NP_001033692.2:p.Ala263=
NM_001244734.2:c.789_811delinsTTGGATCACCACCATTATTATTC NP_001231663.1:p.Ala263=