Canonical Allele Identifier: CA2026372934

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32840954T= , CM000674.2:g.32840954T=	GRCh38
NC_000012.11:g.32993888T= , CM000674.1:g.32993888T=	GRCh37
NC_000012.10:g.32885155T=	NCBI36
NG_009000.1:g.60893A= , LRG_398:g.60893A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700559.2:c.1556+74A=	ENSP00000515065.2:n.1556+74A=
ENST00000700563.2:c.1556+74A=	ENSP00000515066.2:n.1556+74A=
ENST00000700556.1:c.27+74A=
ENST00000700559.1:c.771+74A=
ENST00000700560.1:n.771+74A=
ENST00000700561.1:n.897+74A=
ENST00000700563.1:c.1510+74A=
ENST00000700564.1:n.1560+74A=
ENST00000700565.1:n.1483A=
ENST00000070846.11:c.1688+74A=	ENSP00000070846.6:n.1688+74A=
ENST00000340811.9:c.1556+74A= MANE Select	ENSP00000342800.5:n.1556+74A=
ENST00000070846.10:c.1688+74A=	ENSP00000070846.6:n.1688+74A=
ENST00000340811.8:c.1556+74A=	ENSP00000342800.4:n.1556+74A=
ENST00000613243.1:c.1688+74A=	ENSP00000478295.1:n.1688+74A=
NM_001005242.2:c.1556+74A=	NP_001005242.2:n.1556+74A=
NM_004572.3:c.1688+74A= , LRG_398t1:c.1688+74A=	NP_004563.2:n.1688+74A=
NM_001005242.3:c.1556+74A= MANE Select	NP_001005242.2:n.1556+74A=
NM_004572.4:c.1688+74A=	NP_004563.2:n.1688+74A=