Canonical Allele Identifier: CA253977
Gene: DLL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 6834
ClinVar RCV Id: RCV000007236
dbSNP Id: rs786200903
MyVariant Identifiers: chr19:g.39998025del (hg19) chr19:g.39507385del (hg38)
PubMed: PMID:2805381 PMID:15200511
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507385del , CM000681.2:g.39507385del GRCh38
NC_000019.9:g.39998025del , CM000681.1:g.39998025del GRCh37
NC_000019.8:g.44689865del NCBI36
NG_008256.1:g.13469del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356433.10:c.1440del MANE Select ENSP00000348810.4:p.Pro481ArgfsTer?
ENST00000205143.4:c.1440del ENSP00000205143.3:p.Pro481ArgfsTer?
ENST00000356433.9:c.1440del ENSP00000348810.4:p.Pro481ArgfsTer?
NM_016941.3:c.1440del NP_058637.1:p.Pro481ArgfsTer?
NM_203486.2:c.1440del NP_982353.1:p.Pro481ArgfsTer?
NM_016941.4:c.1440del NP_058637.1:p.Pro481ArgfsTer?
NM_203486.3:c.1440del MANE Select NP_982353.1:p.Pro481ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'