Canonical Allele Identifier: CA1553916779
Gene: MARVELD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.69420020C= , CM000667.2:g.69420020C= GRCh38
NC_000005.9:g.68715847C= , CM000667.1:g.68715847C= GRCh37
NC_000005.8:g.68751603C= NCBI36
NG_017201.1:g.9909C=
NG_017201.2:g.9909C=

Transcript Alleles

HGVS Amino-acid change
ENST00000325631.10:c.635C= MANE Select ENSP00000323264.5:p.Thr212=
ENST00000413223.3:c.635C= ENSP00000398922.2:p.Thr212=
ENST00000436532.7:c.635C= ENSP00000414776.2:p.Thr212=
ENST00000645446.1:c.635C= ENSP00000494616.1:p.Thr212=
ENST00000647531.1:c.635C= ENSP00000493858.1:p.Thr212=
ENST00000325631.9:c.635C= ENSP00000323264.5:p.Thr212=
ENST00000413223.2:c.635C= ENSP00000398922.2:p.Thr212=
ENST00000436532.6:c.635C= ENSP00000414776.2:p.Thr212=
ENST00000454295.6:c.635C= ENSP00000396244.2:p.Thr212=
ENST00000512803.5:c.635C= ENSP00000423490.1:p.Thr212=
NM_001038603.2:c.635C= NP_001033692.2:p.Thr212=
NM_001244734.1:c.635C= NP_001231663.1:p.Thr212=
XM_005248445.3:c.635C= XP_005248502.1:p.Thr212=
XM_005248446.3:c.635C= XP_005248503.1:p.Thr212=
XM_005248447.3:c.635C= XP_005248504.1:p.Thr212=
XM_005248445.4:c.635C= XP_005248502.1:p.Thr212=
XM_005248446.4:c.635C= XP_005248503.1:p.Thr212=
XM_005248447.4:c.635C= XP_005248504.1:p.Thr212=
NM_001038603.3:c.635C= MANE Select NP_001033692.2:p.Thr212=
NM_001244734.2:c.635C= NP_001231663.1:p.Thr212=