Canonical Allele Identifier: CA2026352335

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32878941_32878942delinsAG , CM000674.2:g.32878941_32878942delinsAG	GRCh38
NC_000012.11:g.33031875_33031876delinsAG , CM000674.1:g.33031875_33031876delinsAG	GRCh37
NC_000012.10:g.32923142_32923143delinsAG	NCBI36
NG_009000.1:g.22905_22906delinsCT , LRG_398:g.22905_22906delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700559.2:c.314_315delinsCT	ENSP00000515065.2:p.Pro105=
ENST00000700563.2:c.314_315delinsCT	ENSP00000515066.2:p.Pro105=
ENST00000700563.1:c.268_269delinsCT
ENST00000700564.1:n.318_319delinsCT
ENST00000700565.1:n.167_168delinsCT
ENST00000070846.11:c.314_315delinsCT	ENSP00000070846.6:p.Pro105=
ENST00000340811.9:c.314_315delinsCT MANE Select	ENSP00000342800.5:p.Pro105=
ENST00000070846.10:c.314_315delinsCT	ENSP00000070846.6:p.Pro105=
ENST00000340811.8:c.314_315delinsCT	ENSP00000342800.4:p.Pro105=
ENST00000613243.1:c.314_315delinsCT	ENSP00000478295.1:p.Pro105=
NM_001005242.2:c.314_315delinsCT	NP_001005242.2:p.Pro105=
NM_004572.3:c.314_315delinsCT , LRG_398t1:c.314_315delinsCT	NP_004563.2:p.Pro105=
NM_001005242.3:c.314_315delinsCT MANE Select	NP_001005242.2:p.Pro105=
NM_004572.4:c.314_315delinsCT	NP_004563.2:p.Pro105=