Canonical Allele Identifier: CA2172012893
Gene: DLL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931702T= , CM000677.2:g.40931702T= GRCh38
NC_000015.9:g.41223900T= , CM000677.1:g.41223900T= GRCh37
NC_000015.8:g.39011192T= NCBI36
NG_046974.1:g.7370T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.594T= MANE Select ENSP00000249749.5:p.Tyr198=
ENST00000249749.6:c.594T= ENSP00000249749.5:p.Tyr198=
ENST00000559440.1:n.823T=
NM_019074.3:c.594T= NP_061947.1:p.Tyr198=
NM_019074.4:c.594T= MANE Select NP_061947.1:p.Tyr198=