Canonical Allele Identifier: CA2026396050

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32821340C= , CM000674.2:g.32821340C=	GRCh38
NC_000012.11:g.32974274C= , CM000674.1:g.32974274C=	GRCh37
NC_000012.10:g.32865541C=	NCBI36
NG_009000.1:g.80507G= , LRG_398:g.80507G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700555.2:n.516+16G=
ENST00000700559.2:c.2013+16G=	ENSP00000515065.2:n.2013+16G=
ENST00000700563.2:c.2013+16G=	ENSP00000515066.2:n.2013+16G=
ENST00000546498.2:n.700+16G=
ENST00000549461.2:n.552+16G=
ENST00000700555.1:c.444+16G=	ENSP00000515062.1:n.444+16G=
ENST00000700556.1:c.484+16G=
ENST00000700558.1:n.227+16G=
ENST00000700559.1:c.1228+16G=
ENST00000700560.1:n.1228+16G=
ENST00000700561.1:n.1354+16G=
ENST00000700562.1:n.551+16G=
ENST00000700563.1:c.1967+16G=
ENST00000700564.1:n.2033G=
ENST00000070846.11:c.2145+16G=	ENSP00000070846.6:n.2145+16G=
ENST00000340811.9:c.2013+16G= MANE Select	ENSP00000342800.5:n.2013+16G=
ENST00000070846.10:c.2145+16G=	ENSP00000070846.6:n.2145+16G=
ENST00000340811.8:c.2013+16G=	ENSP00000342800.4:n.2013+16G=
ENST00000549461.1:n.459+16G=
ENST00000552612.5:n.450G=
ENST00000613243.1:c.2145+16G=	ENSP00000478295.1:n.2145+16G=
NM_001005242.2:c.2013+16G=	NP_001005242.2:n.2013+16G=
NM_004572.3:c.2145+16G= , LRG_398t1:c.2145+16G=	NP_004563.2:n.2145+16G=
NM_001005242.3:c.2013+16G= MANE Select	NP_001005242.2:n.2013+16G=
NM_004572.4:c.2145+16G=	NP_004563.2:n.2145+16G=