Canonical Allele Identifier: CA2506217542

Gene: PLCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.16913803G>A , CM000665.2:g.16913803G>A	GRCh38
NC_000003.11:g.16955295G>A , CM000665.1:g.16955295G>A	GRCh37
NC_000003.10:g.16930299G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000615277.5:c.327+28437G>A MANE Select	ENSP00000478458.1:n.327+28437G>A
ENST00000460467.1:n.439-95871G>A
ENST00000615277.4:c.327+28437G>A	ENSP00000478458.1:n.327+28437G>A
NM_001144382.1:c.327+28437G>A	NP_001137854.1:n.327+28437G>A
XM_006713073.2:c.12+14119G>A	XP_006713136.1:n.12+14119G>A
XM_006713073.3:c.12+14119G>A	XP_006713136.1:n.12+14119G>A
XM_017006022.2:c.327+28437G>A	XP_016861511.1:n.327+28437G>A
XM_017006023.1:c.327+28437G>A	XP_016861512.1:n.327+28437G>A
XM_017006024.2:c.327+28437G>A	XP_016861513.1:n.327+28437G>A
XM_017006025.1:c.-156+14119G>A	XP_016861514.1:n.-156+14119G>A
NM_001144382.2:c.327+28437G>A MANE Select	NP_001137854.1:n.327+28437G>A