Canonical Allele Identifier: CA2026373824

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32802334C= , CM000674.2:g.32802334C=	GRCh38
NC_000012.11:g.32955268C= , CM000674.1:g.32955268C=	GRCh37
NC_000012.10:g.32846535C=	NCBI36
NG_009000.1:g.99513G= , LRG_398:g.99513G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.670+69G=
ENST00000700557.2:n.259+69G=
ENST00000700559.2:c.2167+69G=	ENSP00000515065.2:n.2167+69G=
ENST00000546498.2:n.854+69G=
ENST00000549461.2:n.659+116G=
ENST00000700555.1:c.598+69G=	ENSP00000515062.1:n.598+69G=
ENST00000700556.1:c.638+69G=
ENST00000700557.1:c.178+69G=	ENSP00000515064.1:n.178+69G=
ENST00000700558.1:n.381+69G=
ENST00000700559.1:c.1382+69G=
ENST00000700560.1:n.1382+69G=
ENST00000700561.1:n.1508+69G=
ENST00000070846.11:c.2299+69G=	ENSP00000070846.6:n.2299+69G=
ENST00000340811.9:c.2167+69G= MANE Select	ENSP00000342800.5:n.2167+69G=
ENST00000070846.10:c.2299+69G=	ENSP00000070846.6:n.2299+69G=
ENST00000340811.8:c.2167+69G=	ENSP00000342800.4:n.2167+69G=
ENST00000613243.1:c.2299+69G=	ENSP00000478295.1:n.2299+69G=
NM_001005242.2:c.2167+69G=	NP_001005242.2:n.2167+69G=
NM_004572.3:c.2299+69G= , LRG_398t1:c.2299+69G=	NP_004563.2:n.2299+69G=
NM_001005242.3:c.2167+69G= MANE Select	NP_001005242.2:n.2167+69G=
NM_004572.4:c.2299+69G=	NP_004563.2:n.2299+69G=