Canonical Allele Identifier: CA479176245

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32975434T>A (hg19)

Genomic Alleles

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

Transcript Alleles

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