Canonical Allele Identifier: CA2026352536
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32878994A= , CM000674.2:g.32878994A= GRCh38
NC_000012.11:g.33031928A= , CM000674.1:g.33031928A= GRCh37
NC_000012.10:g.32923195A= NCBI36
NG_009000.1:g.22853T= , LRG_398:g.22853T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700559.2:c.262T= ENSP00000515065.2:p.Tyr88=
ENST00000700563.2:c.262T= ENSP00000515066.2:p.Tyr88=
ENST00000700563.1:c.216T=
ENST00000700564.1:n.266T=
ENST00000700565.1:n.115T=
ENST00000070846.11:c.262T= ENSP00000070846.6:p.Tyr88=
ENST00000340811.9:c.262T= MANE Select ENSP00000342800.5:p.Tyr88=
ENST00000070846.10:c.262T= ENSP00000070846.6:p.Tyr88=
ENST00000340811.8:c.262T= ENSP00000342800.4:p.Tyr88=
ENST00000613243.1:c.262T= ENSP00000478295.1:p.Tyr88=
NM_001005242.2:c.262T= NP_001005242.2:p.Tyr88=
NM_004572.3:c.262T= , LRG_398t1:c.262T= NP_004563.2:p.Tyr88=
NM_001005242.3:c.262T= MANE Select NP_001005242.2:p.Tyr88=
NM_004572.4:c.262T= NP_004563.2:p.Tyr88=