Canonical Allele Identifier: CA391807096
Gene: DLL4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.41223899A>C (hg19) chr15:g.40931701A>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000249749.7:c.593A>C MANE Select ENSP00000249749.5:p.Tyr198Ser
ENST00000249749.6:c.593A>C ENSP00000249749.5:p.Tyr198Ser
ENST00000559440.1:n.822A>C
NM_019074.3:c.593A>C NP_061947.1:p.Tyr198Ser
NM_019074.4:c.593A>C MANE Select NP_061947.1:p.Tyr198Ser
Search 100 bp 5'
Search 100 bp 3'