Canonical Allele Identifier: CA1553927629
Gene: MARVELD2 HGNC NCBI

Linked Data

dbSNP Id: rs1767022644

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.69433175_69433176insC , CM000667.2:g.69433175_69433176insC GRCh38
NC_000005.9:g.68729002_68729003insC , CM000667.1:g.68729002_68729003insC GRCh37
NC_000005.8:g.68764758_68764759insC NCBI36
NG_017201.1:g.23064_23065insC
NG_017201.2:g.23064_23065insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000325631.10:c.1503+82_1503+83insC MANE Select ENSP00000323264.5:n.1503+82_1503+83insC
ENST00000413223.3:c.1155+82_1155+83insC ENSP00000398922.2:n.1155+82_1155+83insC
ENST00000436532.7:c.1155+82_1155+83insC ENSP00000414776.2:n.1155+82_1155+83insC
ENST00000645446.1:c.1503+82_1503+83insC ENSP00000494616.1:n.1503+82_1503+83insC
ENST00000647531.1:c.1467+82_1467+83insC ENSP00000493858.1:n.1467+82_1467+83insC
ENST00000325631.9:c.1503+82_1503+83insC ENSP00000323264.5:n.1503+82_1503+83insC
ENST00000413223.2:c.1155+82_1155+83insC ENSP00000398922.2:n.1155+82_1155+83insC
ENST00000436532.6:c.1155+82_1155+83insC ENSP00000414776.2:n.1155+82_1155+83insC
ENST00000454295.6:c.1467+82_1467+83insC ENSP00000396244.2:n.1467+82_1467+83insC
ENST00000512803.5:c.1503+82_1503+83insC ENSP00000423490.1:n.1503+82_1503+83insC
NM_001038603.2:c.1503+82_1503+83insC NP_001033692.2:n.1503+82_1503+83insC
NM_001244734.1:c.1467+82_1467+83insC NP_001231663.1:n.1467+82_1467+83insC
XM_005248445.3:c.1503+82_1503+83insC XP_005248502.1:n.1503+82_1503+83insC
XM_005248446.3:c.1503+82_1503+83insC XP_005248503.1:n.1503+82_1503+83insC
XM_005248447.3:c.1467+82_1467+83insC XP_005248504.1:n.1467+82_1467+83insC
XM_005248445.4:c.1503+82_1503+83insC XP_005248502.1:n.1503+82_1503+83insC
XM_005248446.4:c.1503+82_1503+83insC XP_005248503.1:n.1503+82_1503+83insC
XM_005248447.4:c.1467+82_1467+83insC XP_005248504.1:n.1467+82_1467+83insC
NM_001038603.3:c.1503+82_1503+83insC MANE Select NP_001033692.2:n.1503+82_1503+83insC
NM_001244734.2:c.1467+82_1467+83insC NP_001231663.1:n.1467+82_1467+83insC