Canonical Allele Identifier: CA391807086

Gene: DLL4

Linked Data

• MyVariant Identifiers: chr15:g.41223895C>T (hg19) ; chr15:g.40931697C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40931697C>T , CM000677.2:g.40931697C>T	GRCh38
NC_000015.9:g.41223895C>T , CM000677.1:g.41223895C>T	GRCh37
NC_000015.8:g.39011187C>T	NCBI36
NG_046974.1:g.7365C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249749.7:c.589C>T MANE Select	ENSP00000249749.5:p.His197Tyr
ENST00000249749.6:c.589C>T	ENSP00000249749.5:p.His197Tyr
ENST00000559440.1:n.818C>T
NM_019074.3:c.589C>T	NP_061947.1:p.His197Tyr
NM_019074.4:c.589C>T MANE Select	NP_061947.1:p.His197Tyr