Canonical Allele Identifier: CA1553913218
Gene: MARVELD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.69441848C= , CM000667.2:g.69441848C= GRCh38
NC_000005.9:g.68737675C= , CM000667.1:g.68737675C= GRCh37
NC_000005.8:g.68773431C= NCBI36
NG_017201.1:g.31737C=
NG_017201.2:g.31737C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325631.10:c.*194C= MANE Select ENSP00000323264.5:n.*194C=
ENST00000413223.3:c.*162+32C= ENSP00000398922.2:n.*162+32C=
ENST00000436532.7:c.1523C= ENSP00000414776.2:n.1523C=
ENST00000645446.1:c.*194C= ENSP00000494616.1:n.*194C=
ENST00000647531.1:c.*194C= ENSP00000493858.1:n.*194C=
ENST00000325631.9:c.*194C= ENSP00000323264.5:n.*194C=
ENST00000413223.2:c.*162+32C= ENSP00000398922.2:n.*162+32C=
ENST00000436532.6:c.*194C= ENSP00000414776.2:n.*194C=
ENST00000454295.6:c.*194C= ENSP00000396244.2:n.*194C=
NM_001038603.2:c.*194C= NP_001033692.2:n.*194C=
NM_001244734.1:c.*194C= NP_001231663.1:n.*194C=
XM_005248445.3:c.*194C= XP_005248502.1:n.*194C=
XM_005248446.3:c.*194C= XP_005248503.1:n.*194C=
XM_005248447.3:c.*194C= XP_005248504.1:n.*194C=
XM_005248445.4:c.*194C= XP_005248502.1:n.*194C=
XM_005248446.4:c.*194C= XP_005248503.1:n.*194C=
XM_005248447.4:c.*194C= XP_005248504.1:n.*194C=
NM_001038603.3:c.*194C= MANE Select NP_001033692.2:n.*194C=
NM_001244734.2:c.*194C= NP_001231663.1:n.*194C=