Canonical Allele Identifier: CA2843517871
Gene: DBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48633471dup , CM000681.2:g.48633471dup GRCh38
NC_000019.9:g.49136728dup , CM000681.1:g.49136728dup GRCh37
NC_000019.8:g.53828540dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000222122.10:c.739dup MANE Select ENSP00000222122.4:p.Ile247AsnfsTer10
ENST00000222122.9:c.739dup ENSP00000222122.4:p.Ile247AsnfsTer10
ENST00000593500.1:c.133dup ENSP00000471220.1:p.Ile45AsnfsTer10
ENST00000594723.1:n.2982dup
ENST00000599385.5:c.133dup ENSP00000469426.1:p.Ile45AsnfsTer10
ENST00000601104.1:c.739dup ENSP00000469291.1:p.Ile247AsnfsTer?
NM_001352.4:c.739dup NP_001343.2:p.Ile247AsnfsTer10
XM_017026388.2:c.310dup XP_016881877.1:p.Ile104AsnfsTer10
XR_243907.4:n.1644dup
NM_001352.5:c.739dup MANE Select NP_001343.2:p.Ile247AsnfsTer10