Canonical Allele Identifier: CA1077201762
Gene: MARVELD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.69433155_69433156insGTTTT , CM000667.2:g.69433155_69433156insGTTTT GRCh38
NC_000005.9:g.68728982_68728983insGTTTT , CM000667.1:g.68728982_68728983insGTTTT GRCh37
NC_000005.8:g.68764738_68764739insGTTTT NCBI36
NG_017201.1:g.23044_23045insGTTTT
NG_017201.2:g.23044_23045insGTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000325631.10:c.1503+62_1503+63insGTTTT MANE Select ENSP00000323264.5:n.1503+62_1503+63insGTTTT
ENST00000413223.3:c.1155+62_1155+63insGTTTT ENSP00000398922.2:n.1155+62_1155+63insGTTTT
ENST00000436532.7:c.1155+62_1155+63insGTTTT ENSP00000414776.2:n.1155+62_1155+63insGTTTT
ENST00000645446.1:c.1503+62_1503+63insGTTTT ENSP00000494616.1:n.1503+62_1503+63insGTTTT
ENST00000647531.1:c.1467+62_1467+63insGTTTT ENSP00000493858.1:n.1467+62_1467+63insGTTTT
ENST00000325631.9:c.1503+62_1503+63insGTTTT ENSP00000323264.5:n.1503+62_1503+63insGTTTT
ENST00000413223.2:c.1155+62_1155+63insGTTTT ENSP00000398922.2:n.1155+62_1155+63insGTTTT
ENST00000436532.6:c.1155+62_1155+63insGTTTT ENSP00000414776.2:n.1155+62_1155+63insGTTTT
ENST00000454295.6:c.1467+62_1467+63insGTTTT ENSP00000396244.2:n.1467+62_1467+63insGTTTT
ENST00000512803.5:c.1503+62_1503+63insGTTTT ENSP00000423490.1:n.1503+62_1503+63insGTTTT
NM_001038603.2:c.1503+62_1503+63insGTTTT NP_001033692.2:n.1503+62_1503+63insGTTTT
NM_001244734.1:c.1467+62_1467+63insGTTTT NP_001231663.1:n.1467+62_1467+63insGTTTT
XM_005248445.3:c.1503+62_1503+63insGTTTT XP_005248502.1:n.1503+62_1503+63insGTTTT
XM_005248446.3:c.1503+62_1503+63insGTTTT XP_005248503.1:n.1503+62_1503+63insGTTTT
XM_005248447.3:c.1467+62_1467+63insGTTTT XP_005248504.1:n.1467+62_1467+63insGTTTT
XM_005248445.4:c.1503+62_1503+63insGTTTT XP_005248502.1:n.1503+62_1503+63insGTTTT
XM_005248446.4:c.1503+62_1503+63insGTTTT XP_005248503.1:n.1503+62_1503+63insGTTTT
XM_005248447.4:c.1467+62_1467+63insGTTTT XP_005248504.1:n.1467+62_1467+63insGTTTT
NM_001038603.3:c.1503+62_1503+63insGTTTT MANE Select NP_001033692.2:n.1503+62_1503+63insGTTTT
NM_001244734.2:c.1467+62_1467+63insGTTTT NP_001231663.1:n.1467+62_1467+63insGTTTT