Canonical Allele Identifier: CA902320650

Gene: PLCL2

Linked Data

• dbSNP Id: rs1319837437
• gnomAD v3: 3-16913806-AGAT-A
• gnomAD v4: 3-16913806-AGAT-A
• MyVariant Identifiers: chr3:g.16955299_16955301del (hg19) ; chr3:g.16913807_16913809del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.16913807_16913809del , CM000665.2:g.16913807_16913809del	GRCh38
NC_000003.11:g.16955299_16955301del , CM000665.1:g.16955299_16955301del	GRCh37
NC_000003.10:g.16930303_16930305del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000615277.5:c.327+28441_327+28443del MANE Select	ENSP00000478458.1:n.327+28441_327+28443del
ENST00000460467.1:n.439-95867_439-95865del
ENST00000615277.4:c.327+28441_327+28443del	ENSP00000478458.1:n.327+28441_327+28443del
NM_001144382.1:c.327+28441_327+28443del	NP_001137854.1:n.327+28441_327+28443del
XM_006713073.2:c.12+14123_12+14125del	XP_006713136.1:n.12+14123_12+14125del
XM_006713073.3:c.12+14123_12+14125del	XP_006713136.1:n.12+14123_12+14125del
XM_017006022.2:c.327+28441_327+28443del	XP_016861511.1:n.327+28441_327+28443del
XM_017006023.1:c.327+28441_327+28443del	XP_016861512.1:n.327+28441_327+28443del
XM_017006024.2:c.327+28441_327+28443del	XP_016861513.1:n.327+28441_327+28443del
XM_017006025.1:c.-156+14123_-156+14125del	XP_016861514.1:n.-156+14123_-156+14125del
NM_001144382.2:c.327+28441_327+28443del MANE Select	NP_001137854.1:n.327+28441_327+28443del