Canonical Allele Identifier: CA384362533

Gene: PKP2

Linked Data

• ClinVar Variation Id: 2441851
• ClinVar RCV Id: RCV003148166
• MyVariant Identifiers: chr12:g.32975399A>T (hg19) ; chr12:g.32822465A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822465A>T , CM000674.2:g.32822465A>T	GRCh38
NC_000012.11:g.32975399A>T , CM000674.1:g.32975399A>T	GRCh37
NC_000012.10:g.32866666A>T	NCBI36
NG_009000.1:g.79382T>A , LRG_398:g.79382T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.342+11T>A
ENST00000700559.2:c.1839+2T>A	ENSP00000515065.2:n.1839+2T>A
ENST00000700563.2:c.1839+2T>A	ENSP00000515066.2:n.1839+2T>A
ENST00000546498.2:n.526+2T>A
ENST00000700555.1:c.270+11T>A	ENSP00000515062.1:n.270+11T>A
ENST00000700556.1:c.310+2T>A
ENST00000700559.1:c.1054+2T>A
ENST00000700560.1:n.1054+2T>A
ENST00000700561.1:n.1180+2T>A
ENST00000700563.1:c.1793+2T>A
ENST00000700564.1:n.1843+2T>A
ENST00000070846.11:c.1971+2T>A	ENSP00000070846.6:n.1971+2T>A
ENST00000340811.9:c.1839+2T>A MANE Select	ENSP00000342800.5:n.1839+2T>A
ENST00000070846.10:c.1971+2T>A	ENSP00000070846.6:n.1971+2T>A
ENST00000340811.8:c.1839+2T>A	ENSP00000342800.4:n.1839+2T>A
ENST00000546498.1:n.526+2T>A
ENST00000552612.5:n.260+2T>A
ENST00000613243.1:c.1971+2T>A	ENSP00000478295.1:n.1971+2T>A
NM_001005242.2:c.1839+2T>A	NP_001005242.2:n.1839+2T>A
NM_004572.3:c.1971+2T>A , LRG_398t1:c.1971+2T>A	NP_004563.2:n.1971+2T>A
NM_001005242.3:c.1839+2T>A MANE Select	NP_001005242.2:n.1839+2T>A
NM_004572.4:c.1971+2T>A	NP_004563.2:n.1971+2T>A