Canonical Allele Identifier: CA2172013006
Gene: DLL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931980A= , CM000677.2:g.40931980A= GRCh38
NC_000015.9:g.41224178A= , CM000677.1:g.41224178A= GRCh37
NC_000015.8:g.39011470A= NCBI36
NG_046974.1:g.7648A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.659-191A= MANE Select ENSP00000249749.5:n.659-191A=
ENST00000249749.6:c.659-191A= ENSP00000249749.5:n.659-191A=
ENST00000559440.1:n.888-191A=
NM_019074.3:c.659-191A= NP_061947.1:n.659-191A=
NM_019074.4:c.659-191A= MANE Select NP_061947.1:n.659-191A=