Canonical Allele Identifier: CA1348242077

Gene: PLCL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.16897182_16897185delinsTGTC , CM000665.2:g.16897182_16897185delinsTGTC	GRCh38
NC_000003.11:g.16938680_16938683delinsTGTC , CM000665.1:g.16938680_16938683delinsTGTC	GRCh37
NC_000003.10:g.16913684_16913687delinsTGTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615277.5:c.327+11816_327+11819delinsTGTC MANE Select	ENSP00000478458.1:n.327+11816_327+11819delinsTGTC
ENST00000460467.1:n.438+94094_438+94097delinsTGTC
ENST00000615277.4:c.327+11816_327+11819delinsTGTC	ENSP00000478458.1:n.327+11816_327+11819delinsTGTC
NM_001144382.1:c.327+11816_327+11819delinsTGTC	NP_001137854.1:n.327+11816_327+11819delinsTGTC
XM_006713073.3:c.-2491_-2488delinsTGTC	XP_006713136.1:n.-2491_-2488delinsTGTC
XM_017006022.2:c.327+11816_327+11819delinsTGTC	XP_016861511.1:n.327+11816_327+11819delinsTGTC
XM_017006023.1:c.327+11816_327+11819delinsTGTC	XP_016861512.1:n.327+11816_327+11819delinsTGTC
XM_017006024.2:c.327+11816_327+11819delinsTGTC	XP_016861513.1:n.327+11816_327+11819delinsTGTC
XM_017006025.1:c.-2658_-2655delinsTGTC	XP_016861514.1:n.-2658_-2655delinsTGTC
NM_001144382.2:c.327+11816_327+11819delinsTGTC MANE Select	NP_001137854.1:n.327+11816_327+11819delinsTGTC