Canonical Allele Identifier: CA384364730

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32977025A>C (hg19) ; chr12:g.32824091A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32824091A>C , CM000674.2:g.32824091A>C	GRCh38
NC_000012.11:g.32977025A>C , CM000674.1:g.32977025A>C	GRCh37
NC_000012.10:g.32868292A>C	NCBI36
NG_009000.1:g.77756T>G , LRG_398:g.77756T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.140T>G
ENST00000700559.2:c.1628T>G	ENSP00000515065.2:p.Val543Gly
ENST00000700563.2:c.1628T>G	ENSP00000515066.2:p.Val543Gly
ENST00000546498.2:n.315T>G
ENST00000700555.1:c.68T>G	ENSP00000515062.1:p.Val23Gly
ENST00000700556.1:c.99T>G
ENST00000700559.1:c.843T>G
ENST00000700560.1:n.843T>G
ENST00000700561.1:n.969T>G
ENST00000700563.1:c.1582T>G
ENST00000700564.1:n.1632T>G
ENST00000070846.11:c.1760T>G	ENSP00000070846.6:p.Val587Gly
ENST00000340811.9:c.1628T>G MANE Select	ENSP00000342800.5:p.Val543Gly
ENST00000070846.10:c.1760T>G	ENSP00000070846.6:p.Val587Gly
ENST00000340811.8:c.1628T>G	ENSP00000342800.4:p.Val543Gly
ENST00000546498.1:n.315T>G
ENST00000552612.5:n.49T>G
ENST00000613243.1:c.1760T>G	ENSP00000478295.1:p.Val587Gly
NM_001005242.2:c.1628T>G	NP_001005242.2:p.Val543Gly
NM_004572.3:c.1760T>G , LRG_398t1:c.1760T>G	NP_004563.2:p.Val587Gly
NM_001005242.3:c.1628T>G MANE Select	NP_001005242.2:p.Val543Gly
NM_004572.4:c.1760T>G	NP_004563.2:p.Val587Gly