Canonical Allele Identifier: CA9432075
Gene: DLL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 329230
ClinVar RCV Id: RCV000304748 RCV000399215
dbSNP Id: rs747003629
ExAC: 19:39989596 A / AC
gnomAD v2: 19-39989596-A-AC
gnomAD v3: 19-39498956-A-AC
gnomAD v4: 19-39498956-A-AC
MyVariant Identifiers: chr19:g.39989603dupC (hg19) chr19:g.39989597_39989598insC (hg19) chr19:g.39989596_39989597insC (hg19) chr19:g.39498963dupC (hg38) chr19:g.39498956_39498957insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39498963dup , CM000681.2:g.39498963dup GRCh38
NC_000019.9:g.39989603dup , CM000681.1:g.39989603dup GRCh37
NC_000019.8:g.44681443dup NCBI36
NG_008256.1:g.5047dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356433.10:c.-12dup MANE Select ENSP00000348810.4:n.-12dup
ENST00000356433.9:c.-12dup ENSP00000348810.4:n.-12dup
ENST00000600437.1:n.69dup
NM_016941.3:c.-12dup NP_058637.1:n.-12dup
NM_203486.2:c.-12dup NP_982353.1:n.-12dup
NM_016941.4:c.-12dup NP_058637.1:n.-12dup
NM_203486.3:c.-12dup MANE Select NP_982353.1:n.-12dup
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