Canonical Allele Identifier: CA2674131339

Gene: MARVELD2

Linked Data

• gnomAD v4: 5-69433153-C-CTTTTTTTTTTTTTTTTTTTTTTTGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.69433176_69433177insGTTTTTTTTTTTTTTTTTTTTTTTTT , CM000667.2:g.69433176_69433177insGTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000005.9:g.68729003_68729004insGTTTTTTTTTTTTTTTTTTTTTTTTT , CM000667.1:g.68729003_68729004insGTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000005.8:g.68764759_68764760insGTTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_017201.1:g.23065_23066insGTTTTTTTTTTTTTTTTTTTTTTTTT
NG_017201.2:g.23065_23066insGTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325631.10:c.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000323264.5:n.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000413223.3:c.1155+83_1155+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000398922.2:n.1155+83_1155+84insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000436532.7:c.1155+83_1155+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000414776.2:n.1155+83_1155+84insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000645446.1:c.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000494616.1:n.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000647531.1:c.1467+83_1467+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000493858.1:n.1467+83_1467+84insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000325631.9:c.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000323264.5:n.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000413223.2:c.1155+83_1155+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000398922.2:n.1155+83_1155+84insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000436532.6:c.1155+83_1155+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000414776.2:n.1155+83_1155+84insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000454295.6:c.1467+83_1467+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000396244.2:n.1467+83_1467+84insGTTTTTTTTTTTTTTTTTTTTTT...
ENST00000512803.5:c.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000423490.1:n.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTT...
NM_001038603.2:c.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001033692.2:n.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_001244734.1:c.1467+83_1467+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001231663.1:n.1467+83_1467+84insGTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005248445.3:c.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005248502.1:n.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005248446.3:c.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005248503.1:n.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005248447.3:c.1467+83_1467+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005248504.1:n.1467+83_1467+84insGTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005248445.4:c.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005248502.1:n.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005248446.4:c.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005248503.1:n.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005248447.4:c.1467+83_1467+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005248504.1:n.1467+83_1467+84insGTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_001038603.3:c.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_001033692.2:n.1503+83_1503+84insGTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_001244734.2:c.1467+83_1467+84insGTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001231663.1:n.1467+83_1467+84insGTTTTTTTTTTTTTTTTTTTTTTTTT...