Canonical Allele Identifier: CA919537954
Gene: DLL4 HGNC NCBI

Linked Data

dbSNP Id: rs1596192685
gnomAD v3: 15-40931941-TC-T
gnomAD v4: 15-40931941-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931943del , CM000677.2:g.40931943del GRCh38
NC_000015.9:g.41224141del , CM000677.1:g.41224141del GRCh37
NC_000015.8:g.39011433del NCBI36
NG_046974.1:g.7611del

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.658+177del MANE Select ENSP00000249749.5:n.658+177del
ENST00000249749.6:c.658+177del ENSP00000249749.5:n.658+177del
ENST00000559440.1:n.887+177del
NM_019074.3:c.658+177del NP_061947.1:n.658+177del
NM_019074.4:c.658+177del MANE Select NP_061947.1:n.658+177del
Search 100 bp 5'
Search 100 bp 3'