Canonical Allele Identifier: CA2172013031
Gene: DLL4 HGNC NCBI

Linked Data

dbSNP Id: rs1892777843

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40932044_40932052del , CM000677.2:g.40932044_40932052del GRCh38
NC_000015.9:g.41224242_41224250del , CM000677.1:g.41224242_41224250del GRCh37
NC_000015.8:g.39011534_39011542del NCBI36
NG_046974.1:g.7712_7720del

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.659-127_659-119del MANE Select ENSP00000249749.5:n.659-127_659-119del
ENST00000249749.6:c.659-127_659-119del ENSP00000249749.5:n.659-127_659-119del
ENST00000559440.1:n.888-127_888-119del
NM_019074.3:c.659-127_659-119del NP_061947.1:n.659-127_659-119del
NM_019074.4:c.659-127_659-119del MANE Select NP_061947.1:n.659-127_659-119del