Canonical Allele Identifier: CA1077201786
Gene: MARVELD2 HGNC NCBI

Linked Data

dbSNP Id: rs11345515

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.69433170_69433177dup , CM000667.2:g.69433170_69433177dup GRCh38
NC_000005.9:g.68728997_68729004dup , CM000667.1:g.68728997_68729004dup GRCh37
NC_000005.8:g.68764753_68764760dup NCBI36
NG_017201.1:g.23059_23066dup
NG_017201.2:g.23059_23066dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000325631.10:c.1503+77_1503+84dup MANE Select ENSP00000323264.5:n.1503+77_1503+84dup
ENST00000413223.3:c.1155+77_1155+84dup ENSP00000398922.2:n.1155+77_1155+84dup
ENST00000436532.7:c.1155+77_1155+84dup ENSP00000414776.2:n.1155+77_1155+84dup
ENST00000645446.1:c.1503+77_1503+84dup ENSP00000494616.1:n.1503+77_1503+84dup
ENST00000647531.1:c.1467+77_1467+84dup ENSP00000493858.1:n.1467+77_1467+84dup
ENST00000325631.9:c.1503+77_1503+84dup ENSP00000323264.5:n.1503+77_1503+84dup
ENST00000413223.2:c.1155+77_1155+84dup ENSP00000398922.2:n.1155+77_1155+84dup
ENST00000436532.6:c.1155+77_1155+84dup ENSP00000414776.2:n.1155+77_1155+84dup
ENST00000454295.6:c.1467+77_1467+84dup ENSP00000396244.2:n.1467+77_1467+84dup
ENST00000512803.5:c.1503+77_1503+84dup ENSP00000423490.1:n.1503+77_1503+84dup
NM_001038603.2:c.1503+77_1503+84dup NP_001033692.2:n.1503+77_1503+84dup
NM_001244734.1:c.1467+77_1467+84dup NP_001231663.1:n.1467+77_1467+84dup
XM_005248445.3:c.1503+77_1503+84dup XP_005248502.1:n.1503+77_1503+84dup
XM_005248446.3:c.1503+77_1503+84dup XP_005248503.1:n.1503+77_1503+84dup
XM_005248447.3:c.1467+77_1467+84dup XP_005248504.1:n.1467+77_1467+84dup
XM_005248445.4:c.1503+77_1503+84dup XP_005248502.1:n.1503+77_1503+84dup
XM_005248446.4:c.1503+77_1503+84dup XP_005248503.1:n.1503+77_1503+84dup
XM_005248447.4:c.1467+77_1467+84dup XP_005248504.1:n.1467+77_1467+84dup
NM_001038603.3:c.1503+77_1503+84dup MANE Select NP_001033692.2:n.1503+77_1503+84dup
NM_001244734.2:c.1467+77_1467+84dup NP_001231663.1:n.1467+77_1467+84dup