Canonical Allele Identifier: CA2578876998
Gene: DBNL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44062722dup , CM000669.2:g.44062722dup GRCh38
NC_000007.13:g.44102321dup , CM000669.1:g.44102321dup GRCh37
NC_000007.12:g.44068846dup NCBI36
NG_013016.1:g.7867dup

Transcript Alleles

HGVS Amino-acid change
ENST00000448521.6:c.*1806dup MANE Select ENSP00000411701.1:n.*1806dup
ENST00000432854.5:c.2884dup
NM_001014436.3:c.*1806dup MANE Select NP_001014436.1:n.*1806dup
NM_001122956.2:c.*1806dup NP_001116428.1:n.*1806dup
NM_001284313.2:c.*1806dup NP_001271242.1:n.*1806dup
NM_001362723.2:c.*1806dup NP_001349652.1:n.*1806dup
NM_014063.7:c.*1806dup NP_054782.2:n.*1806dup
NM_001284315.2:c.*1806dup NP_001271244.1:n.*1806dup