Canonical Allele Identifier: CA2026396944

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822500T= , CM000674.2:g.32822500T=	GRCh38
NC_000012.11:g.32975434T= , CM000674.1:g.32975434T=	GRCh37
NC_000012.10:g.32866701T=	NCBI36
NG_009000.1:g.79347A= , LRG_398:g.79347A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700555.2:n.318A=
ENST00000700559.2:c.1806A=	ENSP00000515065.2:p.Gly602=
ENST00000700563.2:c.1806A=	ENSP00000515066.2:p.Gly602=
ENST00000546498.2:n.493A=
ENST00000700555.1:c.246A=	ENSP00000515062.1:p.Gly82=
ENST00000700556.1:c.277A=
ENST00000700559.1:c.1021A=
ENST00000700560.1:n.1021A=
ENST00000700561.1:n.1147A=
ENST00000700563.1:c.1760A=
ENST00000700564.1:n.1810A=
ENST00000070846.11:c.1938A=	ENSP00000070846.6:p.Gly646=
ENST00000340811.9:c.1806A= MANE Select	ENSP00000342800.5:p.Gly602=
ENST00000070846.10:c.1938A=	ENSP00000070846.6:p.Gly646=
ENST00000340811.8:c.1806A=	ENSP00000342800.4:p.Gly602=
ENST00000546498.1:n.493A=
ENST00000552612.5:n.227A=
ENST00000613243.1:c.1938A=	ENSP00000478295.1:p.Gly646=
NM_001005242.2:c.1806A=	NP_001005242.2:p.Gly602=
NM_004572.3:c.1938A= , LRG_398t1:c.1938A=	NP_004563.2:p.Gly646=
NM_001005242.3:c.1806A= MANE Select	NP_001005242.2:p.Gly602=
NM_004572.4:c.1938A=	NP_004563.2:p.Gly646=