Canonical Allele Identifier: CA1348242013
Gene: PLCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.16897094T= , CM000665.2:g.16897094T= GRCh38
NC_000003.11:g.16938592T= , CM000665.1:g.16938592T= GRCh37
NC_000003.10:g.16913596T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000615277.5:c.327+11728T= MANE Select ENSP00000478458.1:n.327+11728T=
ENST00000460467.1:n.438+94006T=
ENST00000615277.4:c.327+11728T= ENSP00000478458.1:n.327+11728T=
NM_001144382.1:c.327+11728T= NP_001137854.1:n.327+11728T=
XM_006713073.3:c.-2579T= XP_006713136.1:n.-2579T=
XM_017006022.2:c.327+11728T= XP_016861511.1:n.327+11728T=
XM_017006023.1:c.327+11728T= XP_016861512.1:n.327+11728T=
XM_017006024.2:c.327+11728T= XP_016861513.1:n.327+11728T=
XM_017006025.1:c.-2746T= XP_016861514.1:n.-2746T=
NM_001144382.2:c.327+11728T= MANE Select NP_001137854.1:n.327+11728T=