Canonical Allele Identifier: CA9432484

Gene: DLL3

Linked Data

• ClinVar Variation Id: 711080
• ClinVar RCV Id: RCV000882778 ; RCV001134423 ; RCV001134424
• dbSNP Id: rs200988915
• ExAC: 19:39998208 G / A
• gnomAD v2: 19-39998208-G-A
• gnomAD v3: 19-39507568-G-A
• gnomAD v4: 19-39507568-G-A
• MyVariant Identifiers: chr19:g.39998208G>A (hg19) ; chr19:g.39507568G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39507568G>A , CM000681.2:g.39507568G>A	GRCh38
NC_000019.9:g.39998208G>A , CM000681.1:g.39998208G>A	GRCh37
NC_000019.8:g.44690048G>A	NCBI36
NG_008256.1:g.13652G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356433.10:c.1623G>A MANE Select	ENSP00000348810.4:p.Pro541=
ENST00000205143.4:c.1623G>A	ENSP00000205143.3:p.Pro541=
ENST00000356433.9:c.1623G>A	ENSP00000348810.4:p.Pro541=
NM_016941.3:c.1623G>A	NP_058637.1:p.Pro541=
NM_203486.2:c.1623G>A	NP_982353.1:p.Pro541=
NM_016941.4:c.1623G>A	NP_058637.1:p.Pro541=
NM_203486.3:c.1623G>A MANE Select	NP_982353.1:p.Pro541=