Canonical Allele Identifier: CA2766863558

Gene: MARVELD2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.69433239_69433240insTTTTTTT , CM000667.2:g.69433239_69433240insTTTTTTT	GRCh38
NC_000005.9:g.68729066_68729067insTTTTTTT , CM000667.1:g.68729066_68729067insTTTTTTT	GRCh37
NC_000005.8:g.68764822_68764823insTTTTTTT	NCBI36
NG_017201.1:g.23128_23129insTTTTTTT
NG_017201.2:g.23128_23129insTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325631.10:c.1503+146_1503+147insTTTTTTT MANE Select	ENSP00000323264.5:n.1503+146_1503+147insTTTTTTT
ENST00000413223.3:c.1155+146_1155+147insTTTTTTT	ENSP00000398922.2:n.1155+146_1155+147insTTTTTTT
ENST00000436532.7:c.1155+146_1155+147insTTTTTTT	ENSP00000414776.2:n.1155+146_1155+147insTTTTTTT
ENST00000645446.1:c.1503+146_1503+147insTTTTTTT	ENSP00000494616.1:n.1503+146_1503+147insTTTTTTT
ENST00000647531.1:c.1467+146_1467+147insTTTTTTT	ENSP00000493858.1:n.1467+146_1467+147insTTTTTTT
ENST00000325631.9:c.1503+146_1503+147insTTTTTTT	ENSP00000323264.5:n.1503+146_1503+147insTTTTTTT
ENST00000413223.2:c.1155+146_1155+147insTTTTTTT	ENSP00000398922.2:n.1155+146_1155+147insTTTTTTT
ENST00000436532.6:c.1155+146_1155+147insTTTTTTT	ENSP00000414776.2:n.1155+146_1155+147insTTTTTTT
ENST00000454295.6:c.1467+146_1467+147insTTTTTTT	ENSP00000396244.2:n.1467+146_1467+147insTTTTTTT
ENST00000512803.5:c.1503+146_1503+147insTTTTTTT	ENSP00000423490.1:n.1503+146_1503+147insTTTTTTT
NM_001038603.2:c.1503+146_1503+147insTTTTTTT	NP_001033692.2:n.1503+146_1503+147insTTTTTTT
NM_001244734.1:c.1467+146_1467+147insTTTTTTT	NP_001231663.1:n.1467+146_1467+147insTTTTTTT
XM_005248445.3:c.1503+146_1503+147insTTTTTTT	XP_005248502.1:n.1503+146_1503+147insTTTTTTT
XM_005248446.3:c.1503+146_1503+147insTTTTTTT	XP_005248503.1:n.1503+146_1503+147insTTTTTTT
XM_005248447.3:c.1467+146_1467+147insTTTTTTT	XP_005248504.1:n.1467+146_1467+147insTTTTTTT
XM_005248445.4:c.1503+146_1503+147insTTTTTTT	XP_005248502.1:n.1503+146_1503+147insTTTTTTT
XM_005248446.4:c.1503+146_1503+147insTTTTTTT	XP_005248503.1:n.1503+146_1503+147insTTTTTTT
XM_005248447.4:c.1467+146_1467+147insTTTTTTT	XP_005248504.1:n.1467+146_1467+147insTTTTTTT
NM_001038603.3:c.1503+146_1503+147insTTTTTTT MANE Select	NP_001033692.2:n.1503+146_1503+147insTTTTTTT
NM_001244734.2:c.1467+146_1467+147insTTTTTTT	NP_001231663.1:n.1467+146_1467+147insTTTTTTT