Canonical Allele Identifier: CA1348241952

Gene: PLCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.16897025T= , CM000665.2:g.16897025T=	GRCh38
NC_000003.11:g.16938523T= , CM000665.1:g.16938523T=	GRCh37
NC_000003.10:g.16913527T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615277.5:c.327+11659T= MANE Select	ENSP00000478458.1:n.327+11659T=
ENST00000460467.1:n.438+93937T=
ENST00000615277.4:c.327+11659T=	ENSP00000478458.1:n.327+11659T=
NM_001144382.1:c.327+11659T=	NP_001137854.1:n.327+11659T=
XM_006713073.3:c.-2648T=	XP_006713136.1:n.-2648T=
XM_017006022.2:c.327+11659T=	XP_016861511.1:n.327+11659T=
XM_017006023.1:c.327+11659T=	XP_016861512.1:n.327+11659T=
XM_017006024.2:c.327+11659T=	XP_016861513.1:n.327+11659T=
XM_017006025.1:c.-2815T=	XP_016861514.1:n.-2815T=
NM_001144382.2:c.327+11659T= MANE Select	NP_001137854.1:n.327+11659T=