Canonical Allele Identifier: CA391807098

Gene: DLL4

Linked Data

• MyVariant Identifiers: chr15:g.41223899A>T (hg19) ; chr15:g.40931701A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40931701A>T , CM000677.2:g.40931701A>T	GRCh38
NC_000015.9:g.41223899A>T , CM000677.1:g.41223899A>T	GRCh37
NC_000015.8:g.39011191A>T	NCBI36
NG_046974.1:g.7369A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249749.7:c.593A>T MANE Select	ENSP00000249749.5:p.Tyr198Phe
ENST00000249749.6:c.593A>T	ENSP00000249749.5:p.Tyr198Phe
ENST00000559440.1:n.822A>T
NM_019074.3:c.593A>T	NP_061947.1:p.Tyr198Phe
NM_019074.4:c.593A>T MANE Select	NP_061947.1:p.Tyr198Phe