Canonical Allele Identifier: CA1348255784

Gene: PLCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.16913795_16913796delinsCT , CM000665.2:g.16913795_16913796delinsCT	GRCh38
NC_000003.11:g.16955287_16955288delinsCT , CM000665.1:g.16955287_16955288delinsCT	GRCh37
NC_000003.10:g.16930291_16930292delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000615277.5:c.327+28429_327+28430delinsCT MANE Select	ENSP00000478458.1:n.327+28429_327+28430delinsCT
ENST00000460467.1:n.439-95879_439-95878delinsCT
ENST00000615277.4:c.327+28429_327+28430delinsCT	ENSP00000478458.1:n.327+28429_327+28430delinsCT
NM_001144382.1:c.327+28429_327+28430delinsCT	NP_001137854.1:n.327+28429_327+28430delinsCT
XM_006713073.2:c.12+14111_12+14112delinsCT	XP_006713136.1:n.12+14111_12+14112delinsCT
XM_006713073.3:c.12+14111_12+14112delinsCT	XP_006713136.1:n.12+14111_12+14112delinsCT
XM_017006022.2:c.327+28429_327+28430delinsCT	XP_016861511.1:n.327+28429_327+28430delinsCT
XM_017006023.1:c.327+28429_327+28430delinsCT	XP_016861512.1:n.327+28429_327+28430delinsCT
XM_017006024.2:c.327+28429_327+28430delinsCT	XP_016861513.1:n.327+28429_327+28430delinsCT
XM_017006025.1:c.-156+14111_-156+14112delinsCT	XP_016861514.1:n.-156+14111_-156+14112delinsCT
NM_001144382.2:c.327+28429_327+28430delinsCT MANE Select	NP_001137854.1:n.327+28429_327+28430delinsCT