Canonical Allele Identifier: CA1553913213
Gene: MARVELD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.69441842G= , CM000667.2:g.69441842G= GRCh38
NC_000005.9:g.68737669G= , CM000667.1:g.68737669G= GRCh37
NC_000005.8:g.68773425G= NCBI36
NG_017201.1:g.31731G=
NG_017201.2:g.31731G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325631.10:c.*188G= MANE Select ENSP00000323264.5:n.*188G=
ENST00000413223.3:c.*162+26G= ENSP00000398922.2:n.*162+26G=
ENST00000436532.7:c.1517G= ENSP00000414776.2:n.1517G=
ENST00000645446.1:c.*188G= ENSP00000494616.1:n.*188G=
ENST00000647531.1:c.*188G= ENSP00000493858.1:n.*188G=
ENST00000325631.9:c.*188G= ENSP00000323264.5:n.*188G=
ENST00000413223.2:c.*162+26G= ENSP00000398922.2:n.*162+26G=
ENST00000436532.6:c.*188G= ENSP00000414776.2:n.*188G=
ENST00000454295.6:c.*188G= ENSP00000396244.2:n.*188G=
NM_001038603.2:c.*188G= NP_001033692.2:n.*188G=
NM_001244734.1:c.*188G= NP_001231663.1:n.*188G=
XM_005248445.3:c.*188G= XP_005248502.1:n.*188G=
XM_005248446.3:c.*188G= XP_005248503.1:n.*188G=
XM_005248447.3:c.*188G= XP_005248504.1:n.*188G=
XM_005248445.4:c.*188G= XP_005248502.1:n.*188G=
XM_005248446.4:c.*188G= XP_005248503.1:n.*188G=
XM_005248447.4:c.*188G= XP_005248504.1:n.*188G=
NM_001038603.3:c.*188G= MANE Select NP_001033692.2:n.*188G=
NM_001244734.2:c.*188G= NP_001231663.1:n.*188G=