Canonical Allele Identifier: CA012436
Gene: PKP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 202014
ClinVar RCV Id: RCV000183784
dbSNP Id: rs794729123

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32878207_32878208del , CM000674.2:g.32878207_32878208del GRCh38
NC_000012.11:g.33031141_33031142del , CM000674.1:g.33031141_33031142del GRCh37
NC_000012.10:g.32922408_32922409del NCBI36
NG_009000.1:g.23641_23642del , LRG_398:g.23641_23642del

Transcript Alleles

HGVS Amino-acid change
ENST00000700559.2:c.674_675del ENSP00000515065.2:p.Ser225CysfsTer2
ENST00000700563.2:c.674_675del ENSP00000515066.2:p.Ser225CysfsTer2
ENST00000700561.1:n.15_16del
ENST00000700563.1:c.628_629del
ENST00000700564.1:n.678_679del
ENST00000700565.1:n.527_528del
ENST00000070846.11:c.674_675del ENSP00000070846.6:p.Ser225CysfsTer2
ENST00000340811.9:c.674_675del MANE Select ENSP00000342800.5:p.Ser225CysfsTer2
ENST00000070846.10:c.674_675del ENSP00000070846.6:p.Ser225CysfsTer2
ENST00000340811.8:c.674_675del ENSP00000342800.4:p.Ser225CysfsTer2
ENST00000613243.1:c.674_675del ENSP00000478295.1:p.Ser225CysfsTer2
NM_001005242.2:c.674_675del NP_001005242.2:p.Ser225CysfsTer2
NM_004572.3:c.674_675del , LRG_398t1:c.674_675del NP_004563.2:p.Ser225CysfsTer2
NM_001005242.3:c.674_675del MANE Select NP_001005242.2:p.Ser225CysfsTer2
NM_004572.4:c.674_675del NP_004563.2:p.Ser225CysfsTer2