Canonical Allele Identifier: CA2172013039
Gene: DLL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40932063A= , CM000677.2:g.40932063A= GRCh38
NC_000015.9:g.41224261A= , CM000677.1:g.41224261A= GRCh37
NC_000015.8:g.39011553A= NCBI36
NG_046974.1:g.7731A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.659-108A= MANE Select ENSP00000249749.5:n.659-108A=
ENST00000249749.6:c.659-108A= ENSP00000249749.5:n.659-108A=
ENST00000559440.1:n.888-108A=
NM_019074.3:c.659-108A= NP_061947.1:n.659-108A=
NM_019074.4:c.659-108A= MANE Select NP_061947.1:n.659-108A=