Canonical Allele Identifier: CA2674131274
Gene: MARVELD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.69433152_69433153insTTT , CM000667.2:g.69433152_69433153insTTT GRCh38
NC_000005.9:g.68728979_68728980insTTT , CM000667.1:g.68728979_68728980insTTT GRCh37
NC_000005.8:g.68764735_68764736insTTT NCBI36
NG_017201.1:g.23041_23042insTTT
NG_017201.2:g.23041_23042insTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000325631.10:c.1503+59_1503+60insTTT MANE Select ENSP00000323264.5:n.1503+59_1503+60insTTT
ENST00000413223.3:c.1155+59_1155+60insTTT ENSP00000398922.2:n.1155+59_1155+60insTTT
ENST00000436532.7:c.1155+59_1155+60insTTT ENSP00000414776.2:n.1155+59_1155+60insTTT
ENST00000645446.1:c.1503+59_1503+60insTTT ENSP00000494616.1:n.1503+59_1503+60insTTT
ENST00000647531.1:c.1467+59_1467+60insTTT ENSP00000493858.1:n.1467+59_1467+60insTTT
ENST00000325631.9:c.1503+59_1503+60insTTT ENSP00000323264.5:n.1503+59_1503+60insTTT
ENST00000413223.2:c.1155+59_1155+60insTTT ENSP00000398922.2:n.1155+59_1155+60insTTT
ENST00000436532.6:c.1155+59_1155+60insTTT ENSP00000414776.2:n.1155+59_1155+60insTTT
ENST00000454295.6:c.1467+59_1467+60insTTT ENSP00000396244.2:n.1467+59_1467+60insTTT
ENST00000512803.5:c.1503+59_1503+60insTTT ENSP00000423490.1:n.1503+59_1503+60insTTT
NM_001038603.2:c.1503+59_1503+60insTTT NP_001033692.2:n.1503+59_1503+60insTTT
NM_001244734.1:c.1467+59_1467+60insTTT NP_001231663.1:n.1467+59_1467+60insTTT
XM_005248445.3:c.1503+59_1503+60insTTT XP_005248502.1:n.1503+59_1503+60insTTT
XM_005248446.3:c.1503+59_1503+60insTTT XP_005248503.1:n.1503+59_1503+60insTTT
XM_005248447.3:c.1467+59_1467+60insTTT XP_005248504.1:n.1467+59_1467+60insTTT
XM_005248445.4:c.1503+59_1503+60insTTT XP_005248502.1:n.1503+59_1503+60insTTT
XM_005248446.4:c.1503+59_1503+60insTTT XP_005248503.1:n.1503+59_1503+60insTTT
XM_005248447.4:c.1467+59_1467+60insTTT XP_005248504.1:n.1467+59_1467+60insTTT
NM_001038603.3:c.1503+59_1503+60insTTT MANE Select NP_001033692.2:n.1503+59_1503+60insTTT
NM_001244734.2:c.1467+59_1467+60insTTT NP_001231663.1:n.1467+59_1467+60insTTT