Canonical Allele Identifier: CA1348255665

Gene: PLCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.16913689_16913695delinsATATATT , CM000665.2:g.16913689_16913695delinsATATATT	GRCh38
NC_000003.11:g.16955181_16955187delinsATATATT , CM000665.1:g.16955181_16955187delinsATATATT	GRCh37
NC_000003.10:g.16930185_16930191delinsATATATT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000615277.5:c.327+28323_327+28329delinsATATATT MANE Select	ENSP00000478458.1:n.327+28323_327+28329delinsATATATT
ENST00000460467.1:n.439-95985_439-95979delinsATATATT
ENST00000615277.4:c.327+28323_327+28329delinsATATATT	ENSP00000478458.1:n.327+28323_327+28329delinsATATATT
NM_001144382.1:c.327+28323_327+28329delinsATATATT	NP_001137854.1:n.327+28323_327+28329delinsATATATT
XM_006713073.2:c.12+14005_12+14011delinsATATATT	XP_006713136.1:n.12+14005_12+14011delinsATATATT
XM_006713073.3:c.12+14005_12+14011delinsATATATT	XP_006713136.1:n.12+14005_12+14011delinsATATATT
XM_017006022.2:c.327+28323_327+28329delinsATATATT	XP_016861511.1:n.327+28323_327+28329delinsATATATT
XM_017006023.1:c.327+28323_327+28329delinsATATATT	XP_016861512.1:n.327+28323_327+28329delinsATATATT
XM_017006024.2:c.327+28323_327+28329delinsATATATT	XP_016861513.1:n.327+28323_327+28329delinsATATATT
XM_017006025.1:c.-156+14005_-156+14011delinsATATATT	XP_016861514.1:n.-156+14005_-156+14011delinsATATATT
NM_001144382.2:c.327+28323_327+28329delinsATATATT MANE Select	NP_001137854.1:n.327+28323_327+28329delinsATATATT