Canonical Allele Identifier: CA507662545
Gene: DLL3 HGNC NCBI

Linked Data

COSMIC: COSM6151130 COSM6151131
MyVariant Identifiers: chr19:g.39998106C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507466C>A , CM000681.2:g.39507466C>A GRCh38
NC_000019.9:g.39998106C>A , CM000681.1:g.39998106C>A GRCh37
NC_000019.8:g.44689946C>A NCBI36
NG_008256.1:g.13550C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356433.10:c.1521C>A MANE Select ENSP00000348810.4:p.Gly507=
ENST00000205143.4:c.1521C>A ENSP00000205143.3:p.Gly507=
ENST00000356433.9:c.1521C>A ENSP00000348810.4:p.Gly507=
NM_016941.3:c.1521C>A NP_058637.1:p.Gly507=
NM_203486.2:c.1521C>A NP_982353.1:p.Gly507=
NM_016941.4:c.1521C>A NP_058637.1:p.Gly507=
NM_203486.3:c.1521C>A MANE Select NP_982353.1:p.Gly507=
Search 100 bp 5'
Search 100 bp 3'