Canonical Allele Identifier: CA2580085379

Gene: PKP2

Linked Data

• ClinVar Variation Id: 2022092
• ClinVar RCV Id: RCV002847512

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32824172A>C , CM000674.2:g.32824172A>C	GRCh38
NC_000012.11:g.32977106A>C , CM000674.1:g.32977106A>C	GRCh37
NC_000012.10:g.32868373A>C	NCBI36
NG_009000.1:g.77675T>G , LRG_398:g.77675T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.69-10T>G
ENST00000700559.2:c.1557-10T>G	ENSP00000515065.2:n.1557-10T>G
ENST00000700563.2:c.1557-10T>G	ENSP00000515066.2:n.1557-10T>G
ENST00000546498.2:n.234T>G
ENST00000700555.1:c.-4-10T>G	ENSP00000515062.1:n.-4-10T>G
ENST00000700556.1:c.28-10T>G
ENST00000700559.1:c.772-10T>G
ENST00000700560.1:n.772-10T>G
ENST00000700561.1:n.898-10T>G
ENST00000700563.1:c.1511-10T>G
ENST00000700564.1:n.1561-10T>G
ENST00000070846.11:c.1689-10T>G	ENSP00000070846.6:n.1689-10T>G
ENST00000340811.9:c.1557-10T>G MANE Select	ENSP00000342800.5:n.1557-10T>G
ENST00000070846.10:c.1689-10T>G	ENSP00000070846.6:n.1689-10T>G
ENST00000340811.8:c.1557-10T>G	ENSP00000342800.4:n.1557-10T>G
ENST00000546498.1:n.234T>G
ENST00000613243.1:c.1689-10T>G	ENSP00000478295.1:n.1689-10T>G
NM_001005242.2:c.1557-10T>G	NP_001005242.2:n.1557-10T>G
NM_004572.3:c.1689-10T>G , LRG_398t1:c.1689-10T>G	NP_004563.2:n.1689-10T>G
NM_001005242.3:c.1557-10T>G MANE Select	NP_001005242.2:n.1557-10T>G
NM_004572.4:c.1689-10T>G	NP_004563.2:n.1689-10T>G