Canonical Allele Identifier: CA1348242087

Gene: PLCL2

Linked Data

• dbSNP Id: rs1696502948

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.16897194G>A , CM000665.2:g.16897194G>A	GRCh38
NC_000003.11:g.16938692G>A , CM000665.1:g.16938692G>A	GRCh37
NC_000003.10:g.16913696G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615277.5:c.327+11828G>A MANE Select	ENSP00000478458.1:n.327+11828G>A
ENST00000460467.1:n.438+94106G>A
ENST00000615277.4:c.327+11828G>A	ENSP00000478458.1:n.327+11828G>A
NM_001144382.1:c.327+11828G>A	NP_001137854.1:n.327+11828G>A
XM_006713073.3:c.-2479G>A	XP_006713136.1:n.-2479G>A
XM_017006022.2:c.327+11828G>A	XP_016861511.1:n.327+11828G>A
XM_017006023.1:c.327+11828G>A	XP_016861512.1:n.327+11828G>A
XM_017006024.2:c.327+11828G>A	XP_016861513.1:n.327+11828G>A
XM_017006025.1:c.-2646G>A	XP_016861514.1:n.-2646G>A
NM_001144382.2:c.327+11828G>A MANE Select	NP_001137854.1:n.327+11828G>A