Canonical Allele Identifier: CA384362734

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32975433A>C (hg19) ; chr12:g.32822499A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822499A>C , CM000674.2:g.32822499A>C	GRCh38
NC_000012.11:g.32975433A>C , CM000674.1:g.32975433A>C	GRCh37
NC_000012.10:g.32866700A>C	NCBI36
NG_009000.1:g.79348T>G , LRG_398:g.79348T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000700555.2:n.319T>G
ENST00000700559.2:c.1807T>G	ENSP00000515065.2:p.Cys603Gly
ENST00000700563.2:c.1807T>G	ENSP00000515066.2:p.Cys603Gly
ENST00000546498.2:n.494T>G
ENST00000700555.1:c.247T>G	ENSP00000515062.1:p.Cys83Gly
ENST00000700556.1:c.278T>G
ENST00000700559.1:c.1022T>G
ENST00000700560.1:n.1022T>G
ENST00000700561.1:n.1148T>G
ENST00000700563.1:c.1761T>G
ENST00000700564.1:n.1811T>G
ENST00000070846.11:c.1939T>G	ENSP00000070846.6:p.Cys647Gly
ENST00000340811.9:c.1807T>G MANE Select	ENSP00000342800.5:p.Cys603Gly
ENST00000070846.10:c.1939T>G	ENSP00000070846.6:p.Cys647Gly
ENST00000340811.8:c.1807T>G	ENSP00000342800.4:p.Cys603Gly
ENST00000546498.1:n.494T>G
ENST00000552612.5:n.228T>G
ENST00000613243.1:c.1939T>G	ENSP00000478295.1:p.Cys647Gly
NM_001005242.2:c.1807T>G	NP_001005242.2:p.Cys603Gly
NM_004572.3:c.1939T>G , LRG_398t1:c.1939T>G	NP_004563.2:p.Cys647Gly
NM_001005242.3:c.1807T>G MANE Select	NP_001005242.2:p.Cys603Gly
NM_004572.4:c.1939T>G	NP_004563.2:p.Cys647Gly