Canonical Allele Identifier: CA1348255766
Gene: PLCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.16913774_16913775delinsAT , CM000665.2:g.16913774_16913775delinsAT GRCh38
NC_000003.11:g.16955266_16955267delinsAT , CM000665.1:g.16955266_16955267delinsAT GRCh37
NC_000003.10:g.16930270_16930271delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000615277.5:c.327+28408_327+28409delinsAT MANE Select ENSP00000478458.1:n.327+28408_327+28409de...
ENST00000460467.1:n.439-95900_439-95899delinsAT
ENST00000615277.4:c.327+28408_327+28409delinsAT ENSP00000478458.1:n.327+28408_327+28409de...
NM_001144382.1:c.327+28408_327+28409delinsAT NP_001137854.1:n.327+28408_327+28409delin...
XM_006713073.2:c.12+14090_12+14091delinsAT XP_006713136.1:n.12+14090_12+14091delinsA...
XM_006713073.3:c.12+14090_12+14091delinsAT XP_006713136.1:n.12+14090_12+14091delinsA...
XM_017006022.2:c.327+28408_327+28409delinsAT XP_016861511.1:n.327+28408_327+28409delin...
XM_017006023.1:c.327+28408_327+28409delinsAT XP_016861512.1:n.327+28408_327+28409delin...
XM_017006024.2:c.327+28408_327+28409delinsAT XP_016861513.1:n.327+28408_327+28409delin...
XM_017006025.1:c.-156+14090_-156+14091delinsAT XP_016861514.1:n.-156+14090_-156+14091del...
NM_001144382.2:c.327+28408_327+28409delinsAT MANE Select NP_001137854.1:n.327+28408_327+28409delin...