Canonical Allele Identifier: CA359924875
Community Standard Title: NM_001038603.3(MARVELD2):c.877G>C (p.Glu293Gln)
Gene: MARVELD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.69420262G>C , CM000667.2:g.69420262G>C GRCh38
NC_000005.9:g.68716089G>C , CM000667.1:g.68716089G>C GRCh37
NC_000005.8:g.68751845G>C NCBI36
NG_017201.1:g.10151G>C
NG_017201.2:g.10151G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001038603.3:c.877G>C MANE Select NP_001033692.2:p.Glu293Gln
ENST00000325631.10:c.877G>C MANE Select ENSP00000323264.5:p.Glu293Gln
NM_001038603.2:c.877G>C NP_001033692.2:p.Glu293Gln
NM_001244734.1:c.877G>C NP_001231663.1:p.Glu293Gln
NM_001244734.2:c.877G>C NP_001231663.1:p.Glu293Gln
ENST00000325631.9:c.877G>C ENSP00000323264.5:p.Glu293Gln
ENST00000413223.2:c.725+152G>C ENSP00000398922.2:n.725+152G>C
ENST00000413223.3:c.725+152G>C ENSP00000398922.2:n.725+152G>C
ENST00000436532.6:c.725+152G>C ENSP00000414776.2:n.725+152G>C
ENST00000436532.7:c.725+152G>C ENSP00000414776.2:n.725+152G>C
ENST00000454295.6:c.877G>C ENSP00000396244.2:p.Glu293Gln
ENST00000512803.5:c.877G>C ENSP00000423490.1:p.Glu293Gln
ENST00000645446.1:c.877G>C ENSP00000494616.1:p.Glu293Gln
ENST00000647531.1:c.877G>C ENSP00000493858.1:p.Glu293Gln
XM_005248445.3:c.877G>C XP_005248502.1:p.Glu293Gln
XM_005248445.4:c.877G>C XP_005248502.1:p.Glu293Gln
XM_005248446.3:c.877G>C XP_005248503.1:p.Glu293Gln
XM_005248446.4:c.877G>C XP_005248503.1:p.Glu293Gln
XM_005248447.3:c.877G>C XP_005248504.1:p.Glu293Gln
XM_005248447.4:c.877G>C XP_005248504.1:p.Glu293Gln