Canonical Allele Identifier: CA2172012855
Gene: DLL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931596C= , CM000677.2:g.40931596C= GRCh38
NC_000015.9:g.41223794C= , CM000677.1:g.41223794C= GRCh37
NC_000015.8:g.39011086C= NCBI36
NG_046974.1:g.7264C=

Transcript Alleles

HGVS Amino-acid change
ENST00000249749.7:c.488C= MANE Select ENSP00000249749.5:p.Thr163=
ENST00000249749.6:c.488C= ENSP00000249749.5:p.Thr163=
ENST00000559440.1:n.717C=
NM_019074.3:c.488C= NP_061947.1:p.Thr163=
NM_019074.4:c.488C= MANE Select NP_061947.1:p.Thr163=