Canonical Allele Identifier: CA2507724309

Gene: PLCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.16897092G>T , CM000665.2:g.16897092G>T	GRCh38
NC_000003.11:g.16938590G>T , CM000665.1:g.16938590G>T	GRCh37
NC_000003.10:g.16913594G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615277.5:c.327+11726G>T MANE Select	ENSP00000478458.1:n.327+11726G>T
ENST00000460467.1:n.438+94004G>T
ENST00000615277.4:c.327+11726G>T	ENSP00000478458.1:n.327+11726G>T
NM_001144382.1:c.327+11726G>T	NP_001137854.1:n.327+11726G>T
XM_006713073.3:c.-2581G>T	XP_006713136.1:n.-2581G>T
XM_017006022.2:c.327+11726G>T	XP_016861511.1:n.327+11726G>T
XM_017006023.1:c.327+11726G>T	XP_016861512.1:n.327+11726G>T
XM_017006024.2:c.327+11726G>T	XP_016861513.1:n.327+11726G>T
XM_017006025.1:c.-2748G>T	XP_016861514.1:n.-2748G>T
NM_001144382.2:c.327+11726G>T MANE Select	NP_001137854.1:n.327+11726G>T