Canonical Allele Identifier: CA2026352169

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32878871T= , CM000674.2:g.32878871T=	GRCh38
NC_000012.11:g.33031805T= , CM000674.1:g.33031805T=	GRCh37
NC_000012.10:g.32923072T=	NCBI36
NG_009000.1:g.22976A= , LRG_398:g.22976A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700559.2:c.336+49A=	ENSP00000515065.2:n.336+49A=
ENST00000700563.2:c.336+49A=	ENSP00000515066.2:n.336+49A=
ENST00000700563.1:c.290+49A=
ENST00000700564.1:n.340+49A=
ENST00000700565.1:n.189+49A=
ENST00000070846.11:c.336+49A=	ENSP00000070846.6:n.336+49A=
ENST00000340811.9:c.336+49A= MANE Select	ENSP00000342800.5:n.336+49A=
ENST00000070846.10:c.336+49A=	ENSP00000070846.6:n.336+49A=
ENST00000340811.8:c.336+49A=	ENSP00000342800.4:n.336+49A=
ENST00000613243.1:c.336+49A=	ENSP00000478295.1:n.336+49A=
NM_001005242.2:c.336+49A=	NP_001005242.2:n.336+49A=
NM_004572.3:c.336+49A= , LRG_398t1:c.336+49A=	NP_004563.2:n.336+49A=
NM_001005242.3:c.336+49A= MANE Select	NP_001005242.2:n.336+49A=
NM_004572.4:c.336+49A=	NP_004563.2:n.336+49A=