Canonical Allele Identifier: CA1703602901

Gene: DBNL

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44062726_44062728delinsCTG , CM000669.2:g.44062726_44062728delinsCTG	GRCh38
NC_000007.13:g.44102325_44102327delinsCTG , CM000669.1:g.44102325_44102327delinsCTG	GRCh37
NC_000007.12:g.44068850_44068852delinsCTG	NCBI36
NG_013016.1:g.7860_7862delinsCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000448521.6:c.*1810_*1812delinsCTG MANE Select	ENSP00000411701.1:n.*1810_*1812delinsCTG
ENST00000432854.5:c.2888_2890delinsCTG
NM_001014436.3:c.*1810_*1812delinsCTG MANE Select	NP_001014436.1:n.*1810_*1812delinsCTG
NM_001122956.2:c.*1810_*1812delinsCTG	NP_001116428.1:n.*1810_*1812delinsCTG
NM_001284313.2:c.*1810_*1812delinsCTG	NP_001271242.1:n.*1810_*1812delinsCTG
NM_001362723.2:c.*1810_*1812delinsCTG	NP_001349652.1:n.*1810_*1812delinsCTG
NM_014063.7:c.*1810_*1812delinsCTG	NP_054782.2:n.*1810_*1812delinsCTG
NM_001284315.2:c.*1810_*1812delinsCTG	NP_001271244.1:n.*1810_*1812delinsCTG