Canonical Allele Identifier: CA1553917307
Gene: MARVELD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.69420391C= , CM000667.2:g.69420391C= GRCh38
NC_000005.9:g.68716218C= , CM000667.1:g.68716218C= GRCh37
NC_000005.8:g.68751974C= NCBI36
NG_017201.1:g.10280C=
NG_017201.2:g.10280C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325631.10:c.1006C= MANE Select ENSP00000323264.5:p.Arg336=
ENST00000413223.3:c.726-68C= ENSP00000398922.2:n.726-68C=
ENST00000436532.7:c.726-68C= ENSP00000414776.2:n.726-68C=
ENST00000645446.1:c.1006C= ENSP00000494616.1:p.Arg336=
ENST00000647531.1:c.1006C= ENSP00000493858.1:p.Arg336=
ENST00000325631.9:c.1006C= ENSP00000323264.5:p.Arg336=
ENST00000413223.2:c.726-68C= ENSP00000398922.2:n.726-68C=
ENST00000436532.6:c.726-68C= ENSP00000414776.2:n.726-68C=
ENST00000454295.6:c.1006C= ENSP00000396244.2:p.Arg336=
ENST00000512803.5:c.1006C= ENSP00000423490.1:p.Arg336=
NM_001038603.2:c.1006C= NP_001033692.2:p.Arg336=
NM_001244734.1:c.1006C= NP_001231663.1:p.Arg336=
XM_005248445.3:c.1006C= XP_005248502.1:p.Arg336=
XM_005248446.3:c.1006C= XP_005248503.1:p.Arg336=
XM_005248447.3:c.1006C= XP_005248504.1:p.Arg336=
XM_005248445.4:c.1006C= XP_005248502.1:p.Arg336=
XM_005248446.4:c.1006C= XP_005248503.1:p.Arg336=
XM_005248447.4:c.1006C= XP_005248504.1:p.Arg336=
NM_001038603.3:c.1006C= MANE Select NP_001033692.2:p.Arg336=
NM_001244734.2:c.1006C= NP_001231663.1:p.Arg336=