Canonical Allele Identifier: CA405788789
Gene: DLL3 HGNC NCBI

Linked Data

gnomAD v4: 19-39507392-C-A
MyVariant Identifiers: chr19:g.39998032C>A (hg19) chr19:g.39507392C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.39507392C>A , CM000681.2:g.39507392C>A GRCh38
NC_000019.9:g.39998032C>A , CM000681.1:g.39998032C>A GRCh37
NC_000019.8:g.44689872C>A NCBI36
NG_008256.1:g.13476C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356433.10:c.1447C>A MANE Select ENSP00000348810.4:p.Leu483Ile
ENST00000205143.4:c.1447C>A ENSP00000205143.3:p.Leu483Ile
ENST00000356433.9:c.1447C>A ENSP00000348810.4:p.Leu483Ile
NM_016941.3:c.1447C>A NP_058637.1:p.Leu483Ile
NM_203486.2:c.1447C>A NP_982353.1:p.Leu483Ile
NM_016941.4:c.1447C>A NP_058637.1:p.Leu483Ile
NM_203486.3:c.1447C>A MANE Select NP_982353.1:p.Leu483Ile
Search 100 bp 5'
Search 100 bp 3'