Canonical Allele Identifier: CA384363565

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32975545G>T (hg19) ; chr12:g.32822611G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822611G>T , CM000674.2:g.32822611G>T	GRCh38
NC_000012.11:g.32975545G>T , CM000674.1:g.32975545G>T	GRCh37
NC_000012.10:g.32866812G>T	NCBI36
NG_009000.1:g.79236C>A , LRG_398:g.79236C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.207C>A
ENST00000700559.2:c.1695C>A	ENSP00000515065.2:p.Cys565Ter
ENST00000700563.2:c.1695C>A	ENSP00000515066.2:p.Cys565Ter
ENST00000546498.2:n.382C>A
ENST00000700555.1:c.135C>A	ENSP00000515062.1:p.Cys45Ter
ENST00000700556.1:c.166C>A
ENST00000700559.1:c.910C>A
ENST00000700560.1:n.910C>A
ENST00000700561.1:n.1036C>A
ENST00000700563.1:c.1649C>A
ENST00000700564.1:n.1699C>A
ENST00000070846.11:c.1827C>A	ENSP00000070846.6:p.Cys609Ter
ENST00000340811.9:c.1695C>A MANE Select	ENSP00000342800.5:p.Cys565Ter
ENST00000070846.10:c.1827C>A	ENSP00000070846.6:p.Cys609Ter
ENST00000340811.8:c.1695C>A	ENSP00000342800.4:p.Cys565Ter
ENST00000546498.1:n.382C>A
ENST00000552612.5:n.116C>A
ENST00000613243.1:c.1827C>A	ENSP00000478295.1:p.Cys609Ter
NM_001005242.2:c.1695C>A	NP_001005242.2:p.Cys565Ter
NM_004572.3:c.1827C>A , LRG_398t1:c.1827C>A	NP_004563.2:p.Cys609Ter
NM_001005242.3:c.1695C>A MANE Select	NP_001005242.2:p.Cys565Ter
NM_004572.4:c.1827C>A	NP_004563.2:p.Cys609Ter