Canonical Allele Identifier: CA1348255759

Gene: PLCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.16913768_16913771delinsATCT , CM000665.2:g.16913768_16913771delinsATCT	GRCh38
NC_000003.11:g.16955260_16955263delinsATCT , CM000665.1:g.16955260_16955263delinsATCT	GRCh37
NC_000003.10:g.16930264_16930267delinsATCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000615277.5:c.327+28402_327+28405delinsATCT MANE Select	ENSP00000478458.1:n.327+28402_327+28405delinsATCT
ENST00000460467.1:n.439-95906_439-95903delinsATCT
ENST00000615277.4:c.327+28402_327+28405delinsATCT	ENSP00000478458.1:n.327+28402_327+28405delinsATCT
NM_001144382.1:c.327+28402_327+28405delinsATCT	NP_001137854.1:n.327+28402_327+28405delinsATCT
XM_006713073.2:c.12+14084_12+14087delinsATCT	XP_006713136.1:n.12+14084_12+14087delinsATCT
XM_006713073.3:c.12+14084_12+14087delinsATCT	XP_006713136.1:n.12+14084_12+14087delinsATCT
XM_017006022.2:c.327+28402_327+28405delinsATCT	XP_016861511.1:n.327+28402_327+28405delinsATCT
XM_017006023.1:c.327+28402_327+28405delinsATCT	XP_016861512.1:n.327+28402_327+28405delinsATCT
XM_017006024.2:c.327+28402_327+28405delinsATCT	XP_016861513.1:n.327+28402_327+28405delinsATCT
XM_017006025.1:c.-156+14084_-156+14087delinsATCT	XP_016861514.1:n.-156+14084_-156+14087delinsATCT
NM_001144382.2:c.327+28402_327+28405delinsATCT MANE Select	NP_001137854.1:n.327+28402_327+28405delinsATCT