Canonical Allele Identifier: CA391807074
Gene: DLL4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.41223890T>A (hg19) chr15:g.40931692T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40931692T>A , CM000677.2:g.40931692T>A GRCh38
NC_000015.9:g.41223890T>A , CM000677.1:g.41223890T>A GRCh37
NC_000015.8:g.39011182T>A NCBI36
NG_046974.1:g.7360T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.584T>A MANE Select ENSP00000249749.5:p.Phe195Tyr
ENST00000249749.6:c.584T>A ENSP00000249749.5:p.Phe195Tyr
ENST00000559440.1:n.813T>A
NM_019074.3:c.584T>A NP_061947.1:p.Phe195Tyr
NM_019074.4:c.584T>A MANE Select NP_061947.1:p.Phe195Tyr
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