Canonical Allele Identifier: CA1553915880
Gene: MARVELD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.69419582_69419585delinsCAGA , CM000667.2:g.69419582_69419585delinsCAGA GRCh38
NC_000005.9:g.68715409_68715412delinsCAGA , CM000667.1:g.68715409_68715412delinsCAGA GRCh37
NC_000005.8:g.68751165_68751168delinsCAGA NCBI36
NG_017201.1:g.9471_9474delinsCAGA
NG_017201.2:g.9471_9474delinsCAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000325631.10:c.197_200delinsCAGA MANE Select ENSP00000323264.5:p.Thr66=
ENST00000413223.3:c.197_200delinsCAGA ENSP00000398922.2:p.Thr66=
ENST00000436532.7:c.197_200delinsCAGA ENSP00000414776.2:p.Thr66=
ENST00000645446.1:c.197_200delinsCAGA ENSP00000494616.1:p.Thr66=
ENST00000647531.1:c.197_200delinsCAGA ENSP00000493858.1:p.Thr66=
ENST00000325631.9:c.197_200delinsCAGA ENSP00000323264.5:p.Thr66=
ENST00000413223.2:c.197_200delinsCAGA ENSP00000398922.2:p.Thr66=
ENST00000436532.6:c.197_200delinsCAGA ENSP00000414776.2:p.Thr66=
ENST00000454295.6:c.197_200delinsCAGA ENSP00000396244.2:p.Thr66=
ENST00000512803.5:c.197_200delinsCAGA ENSP00000423490.1:p.Thr66=
ENST00000515844.1:c.197_200delinsCAGA ENSP00000421902.1:p.Thr66=
NM_001038603.2:c.197_200delinsCAGA NP_001033692.2:p.Thr66=
NM_001244734.1:c.197_200delinsCAGA NP_001231663.1:p.Thr66=
XM_005248445.3:c.197_200delinsCAGA XP_005248502.1:p.Thr66=
XM_005248446.3:c.197_200delinsCAGA XP_005248503.1:p.Thr66=
XM_005248447.3:c.197_200delinsCAGA XP_005248504.1:p.Thr66=
XM_005248445.4:c.197_200delinsCAGA XP_005248502.1:p.Thr66=
XM_005248446.4:c.197_200delinsCAGA XP_005248503.1:p.Thr66=
XM_005248447.4:c.197_200delinsCAGA XP_005248504.1:p.Thr66=
NM_001038603.3:c.197_200delinsCAGA MANE Select NP_001033692.2:p.Thr66=
NM_001244734.2:c.197_200delinsCAGA NP_001231663.1:p.Thr66=