Canonical Allele Identifier: CA9432441

Gene: DLL3

Linked Data

• ClinVar Variation Id: 893400
• ClinVar RCV Id: RCV001131440 ; RCV001131441 ; RCV003106125
• dbSNP Id: rs773460228
• ExAC: 19:39998026 C / G
• gnomAD v2: 19-39998026-C-G
• gnomAD v3: 19-39507386-C-G
• gnomAD v4: 19-39507386-C-G
• MyVariant Identifiers: chr19:g.39998026C>G (hg19) ; chr19:g.39507386C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39507386C>G , CM000681.2:g.39507386C>G	GRCh38
NC_000019.9:g.39998026C>G , CM000681.1:g.39998026C>G	GRCh37
NC_000019.8:g.44689866C>G	NCBI36
NG_008256.1:g.13470C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356433.10:c.1441C>G MANE Select	ENSP00000348810.4:p.Pro481Ala
ENST00000205143.4:c.1441C>G	ENSP00000205143.3:p.Pro481Ala
ENST00000356433.9:c.1441C>G	ENSP00000348810.4:p.Pro481Ala
NM_016941.3:c.1441C>G	NP_058637.1:p.Pro481Ala
NM_203486.2:c.1441C>G	NP_982353.1:p.Pro481Ala
NM_016941.4:c.1441C>G	NP_058637.1:p.Pro481Ala
NM_203486.3:c.1441C>G MANE Select	NP_982353.1:p.Pro481Ala