Canonical Allele Identifier: CA384363421

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32975528G>C (hg19) ; chr12:g.32822594G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822594G>C , CM000674.2:g.32822594G>C	GRCh38
NC_000012.11:g.32975528G>C , CM000674.1:g.32975528G>C	GRCh37
NC_000012.10:g.32866795G>C	NCBI36
NG_009000.1:g.79253C>G , LRG_398:g.79253C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.224C>G
ENST00000700559.2:c.1712C>G	ENSP00000515065.2:p.Ser571Cys
ENST00000700563.2:c.1712C>G	ENSP00000515066.2:p.Ser571Cys
ENST00000546498.2:n.399C>G
ENST00000700555.1:c.152C>G	ENSP00000515062.1:p.Ser51Cys
ENST00000700556.1:c.183C>G
ENST00000700559.1:c.927C>G
ENST00000700560.1:n.927C>G
ENST00000700561.1:n.1053C>G
ENST00000700563.1:c.1666C>G
ENST00000700564.1:n.1716C>G
ENST00000070846.11:c.1844C>G	ENSP00000070846.6:p.Ser615Cys
ENST00000340811.9:c.1712C>G MANE Select	ENSP00000342800.5:p.Ser571Cys
ENST00000070846.10:c.1844C>G	ENSP00000070846.6:p.Ser615Cys
ENST00000340811.8:c.1712C>G	ENSP00000342800.4:p.Ser571Cys
ENST00000546498.1:n.399C>G
ENST00000552612.5:n.133C>G
ENST00000613243.1:c.1844C>G	ENSP00000478295.1:p.Ser615Cys
NM_001005242.2:c.1712C>G	NP_001005242.2:p.Ser571Cys
NM_004572.3:c.1844C>G , LRG_398t1:c.1844C>G	NP_004563.2:p.Ser615Cys
NM_001005242.3:c.1712C>G MANE Select	NP_001005242.2:p.Ser571Cys
NM_004572.4:c.1844C>G	NP_004563.2:p.Ser615Cys