Canonical Allele Identifier: CA2026389104
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32850564_32850565delinsTC , CM000674.2:g.32850564_32850565delinsTC GRCh38
NC_000012.11:g.33003498_33003499delinsTC , CM000674.1:g.33003498_33003499delinsTC GRCh37
NC_000012.10:g.32894765_32894766delinsTC NCBI36
NG_009000.1:g.51282_51283delinsGA , LRG_398:g.51282_51283delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700559.2:c.1378+201_1378+202delinsGA ENSP00000515065.2:n.1378+201_1378+202delinsGA
ENST00000700563.2:c.1378+201_1378+202delinsGA ENSP00000515066.2:n.1378+201_1378+202delinsGA
ENST00000700559.1:c.593+201_593+202delinsGA
ENST00000700560.1:n.593+201_593+202delinsGA
ENST00000700561.1:n.719+201_719+202delinsGA
ENST00000700563.1:c.1332+201_1332+202delinsGA
ENST00000700564.1:n.1382+201_1382+202delinsGA
ENST00000700565.1:n.1231+201_1231+202delinsGA
ENST00000070846.11:c.1378+201_1378+202delinsGA ENSP00000070846.6:n.1378+201_1378+202delinsGA
ENST00000340811.9:c.1378+201_1378+202delinsGA MANE Select ENSP00000342800.5:n.1378+201_1378+202delinsGA
ENST00000070846.10:c.1378+201_1378+202delinsGA ENSP00000070846.6:n.1378+201_1378+202delinsGA
ENST00000340811.8:c.1378+201_1378+202delinsGA ENSP00000342800.4:n.1378+201_1378+202delinsGA
ENST00000613243.1:c.1378+201_1378+202delinsGA ENSP00000478295.1:n.1378+201_1378+202delinsGA
NM_001005242.2:c.1378+201_1378+202delinsGA NP_001005242.2:n.1378+201_1378+202delinsGA
NM_004572.3:c.1378+201_1378+202delinsGA , LRG_398t1:c.1378+201_1378+202delinsGA NP_004563.2:n.1378+201_1378+202delinsGA
NM_001005242.3:c.1378+201_1378+202delinsGA MANE Select NP_001005242.2:n.1378+201_1378+202delinsGA
NM_004572.4:c.1378+201_1378+202delinsGA NP_004563.2:n.1378+201_1378+202delinsGA