Canonical Allele Identifier: CA813514911

Gene: MARVELD2

Linked Data

• dbSNP Id: rs1051809388
• gnomAD v3: 5-69441835-G-A
• gnomAD v4: 5-69441835-G-A
• MyVariant Identifiers: chr5:g.68737662G>A (hg19) ; chr5:g.69441835G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.69441835G>A , CM000667.2:g.69441835G>A	GRCh38
NC_000005.9:g.68737662G>A , CM000667.1:g.68737662G>A	GRCh37
NC_000005.8:g.68773418G>A	NCBI36
NG_017201.1:g.31724G>A
NG_017201.2:g.31724G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325631.10:c.*181G>A MANE Select	ENSP00000323264.5:n.*181G>A
ENST00000413223.3:c.*162+19G>A	ENSP00000398922.2:n.*162+19G>A
ENST00000436532.7:c.1510G>A	ENSP00000414776.2:n.1510G>A
ENST00000645446.1:c.*181G>A	ENSP00000494616.1:n.*181G>A
ENST00000647531.1:c.*181G>A	ENSP00000493858.1:n.*181G>A
ENST00000325631.9:c.*181G>A	ENSP00000323264.5:n.*181G>A
ENST00000413223.2:c.*162+19G>A	ENSP00000398922.2:n.*162+19G>A
ENST00000436532.6:c.*181G>A	ENSP00000414776.2:n.*181G>A
ENST00000454295.6:c.*181G>A	ENSP00000396244.2:n.*181G>A
NM_001038603.2:c.*181G>A	NP_001033692.2:n.*181G>A
NM_001244734.1:c.*181G>A	NP_001231663.1:n.*181G>A
XM_005248445.3:c.*181G>A	XP_005248502.1:n.*181G>A
XM_005248446.3:c.*181G>A	XP_005248503.1:n.*181G>A
XM_005248447.3:c.*181G>A	XP_005248504.1:n.*181G>A
XM_005248445.4:c.*181G>A	XP_005248502.1:n.*181G>A
XM_005248446.4:c.*181G>A	XP_005248503.1:n.*181G>A
XM_005248447.4:c.*181G>A	XP_005248504.1:n.*181G>A
NM_001038603.3:c.*181G>A MANE Select	NP_001033692.2:n.*181G>A
NM_001244734.2:c.*181G>A	NP_001231663.1:n.*181G>A