Canonical Allele Identifier: CA2499225484
Gene: DLL3 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39504071_39504072delinsCT , CM000681.2:g.39504071_39504072delinsCT GRCh38
NC_000019.9:g.39994711_39994712delinsCT , CM000681.1:g.39994711_39994712delinsCT GRCh37
NC_000019.8:g.44686551_44686552delinsCT NCBI36
NG_008256.1:g.10155_10156delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356433.10:c.653_654delinsCT MANE Select ENSP00000348810.4:p.Leu218Pro
ENST00000205143.4:c.653_654delinsCT ENSP00000205143.3:p.Leu218Pro
ENST00000356433.9:c.653_654delinsCT ENSP00000348810.4:p.Leu218Pro
ENST00000596614.5:c.410-2968_410-2967delinsCT ENSP00000471688.1:n.410-2968_410-2967delinsCT
ENST00000600437.1:n.733_734delinsCT
NM_016941.3:c.653_654delinsCT NP_058637.1:p.Leu218Pro
NM_203486.2:c.653_654delinsCT NP_982353.1:p.Leu218Pro
NM_016941.4:c.653_654delinsCT NP_058637.1:p.Leu218Pro
NM_203486.3:c.653_654delinsCT MANE Select NP_982353.1:p.Leu218Pro