Canonical Allele Identifier: CA1553917580
Gene: MARVELD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.69420612C= , CM000667.2:g.69420612C= GRCh38
NC_000005.9:g.68716439C= , CM000667.1:g.68716439C= GRCh37
NC_000005.8:g.68752195C= NCBI36
NG_017201.1:g.10501C=
NG_017201.2:g.10501C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325631.10:c.1146+81C= MANE Select ENSP00000323264.5:n.1146+81C=
ENST00000413223.3:c.798+81C= ENSP00000398922.2:n.798+81C=
ENST00000436532.7:c.798+81C= ENSP00000414776.2:n.798+81C=
ENST00000645446.1:c.1146+81C= ENSP00000494616.1:n.1146+81C=
ENST00000647531.1:c.1146+81C= ENSP00000493858.1:n.1146+81C=
ENST00000325631.9:c.1146+81C= ENSP00000323264.5:n.1146+81C=
ENST00000413223.2:c.798+81C= ENSP00000398922.2:n.798+81C=
ENST00000436532.6:c.798+81C= ENSP00000414776.2:n.798+81C=
ENST00000454295.6:c.1146+81C= ENSP00000396244.2:n.1146+81C=
ENST00000512803.5:c.1146+81C= ENSP00000423490.1:n.1146+81C=
NM_001038603.2:c.1146+81C= NP_001033692.2:n.1146+81C=
NM_001244734.1:c.1146+81C= NP_001231663.1:n.1146+81C=
XM_005248445.3:c.1146+81C= XP_005248502.1:n.1146+81C=
XM_005248446.3:c.1146+81C= XP_005248503.1:n.1146+81C=
XM_005248447.3:c.1146+81C= XP_005248504.1:n.1146+81C=
XM_005248445.4:c.1146+81C= XP_005248502.1:n.1146+81C=
XM_005248446.4:c.1146+81C= XP_005248503.1:n.1146+81C=
XM_005248447.4:c.1146+81C= XP_005248504.1:n.1146+81C=
NM_001038603.3:c.1146+81C= MANE Select NP_001033692.2:n.1146+81C=
NM_001244734.2:c.1146+81C= NP_001231663.1:n.1146+81C=