Canonical Allele Identifier: CA2026390152
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32851303_32851304delinsGA , CM000674.2:g.32851303_32851304delinsGA GRCh38
NC_000012.11:g.33004237_33004238delinsGA , CM000674.1:g.33004237_33004238delinsGA GRCh37
NC_000012.10:g.32895504_32895505delinsGA NCBI36
NG_009000.1:g.50543_50544delinsTC , LRG_398:g.50543_50544delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700559.2:c.1171-331_1171-330delinsTC ENSP00000515065.2:n.1171-331_1171-330delinsTC
ENST00000700563.2:c.1171-331_1171-330delinsTC ENSP00000515066.2:n.1171-331_1171-330delinsTC
ENST00000700559.1:c.386-331_386-330delinsTC
ENST00000700560.1:n.386-331_386-330delinsTC
ENST00000700561.1:n.512-331_512-330delinsTC
ENST00000700563.1:c.1125-331_1125-330delinsTC
ENST00000700564.1:n.1175-331_1175-330delinsTC
ENST00000700565.1:n.1024-331_1024-330delinsTC
ENST00000070846.11:c.1171-331_1171-330delinsTC ENSP00000070846.6:n.1171-331_1171-330delinsTC
ENST00000340811.9:c.1171-331_1171-330delinsTC MANE Select ENSP00000342800.5:n.1171-331_1171-330delinsTC
ENST00000070846.10:c.1171-331_1171-330delinsTC ENSP00000070846.6:n.1171-331_1171-330delinsTC
ENST00000340811.8:c.1171-331_1171-330delinsTC ENSP00000342800.4:n.1171-331_1171-330delinsTC
ENST00000613243.1:c.1171-331_1171-330delinsTC ENSP00000478295.1:n.1171-331_1171-330delinsTC
NM_001005242.2:c.1171-331_1171-330delinsTC NP_001005242.2:n.1171-331_1171-330delinsTC
NM_004572.3:c.1171-331_1171-330delinsTC , LRG_398t1:c.1171-331_1171-330delinsTC NP_004563.2:n.1171-331_1171-330delinsTC
NM_001005242.3:c.1171-331_1171-330delinsTC MANE Select NP_001005242.2:n.1171-331_1171-330delinsTC
NM_004572.4:c.1171-331_1171-330delinsTC NP_004563.2:n.1171-331_1171-330delinsTC