Canonical Allele Identifier: CA882154570

Gene: DLL3

Linked Data

• dbSNP Id: rs1277167365
• gnomAD v4: 19-39507240-CGTGCGCCGCGCGCCCCT-C
• MyVariant Identifiers: chr19:g.39997881_39997897del (hg19) ; chr19:g.39507241_39507257del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.39507245_39507261del , CM000681.2:g.39507245_39507261del	GRCh38
NC_000019.9:g.39997885_39997901del , CM000681.1:g.39997885_39997901del	GRCh37
NC_000019.8:g.44689725_44689741del	NCBI36
NG_008256.1:g.13329_13345del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356433.10:c.1300_1316del MANE Select	ENSP00000348810.4:p.Ala434SerfsTer26
ENST00000205143.4:c.1300_1316del	ENSP00000205143.3:p.Ala434SerfsTer26
ENST00000356433.9:c.1300_1316del	ENSP00000348810.4:p.Ala434SerfsTer26
ENST00000596614.5:c.616_632del	ENSP00000471688.1:p.Ala206SerfsTer?
NM_016941.3:c.1300_1316del	NP_058637.1:p.Ala434SerfsTer26
NM_203486.2:c.1300_1316del	NP_982353.1:p.Ala434SerfsTer26
NM_016941.4:c.1300_1316del	NP_058637.1:p.Ala434SerfsTer26
NM_203486.3:c.1300_1316del MANE Select	NP_982353.1:p.Ala434SerfsTer26