Canonical Allele Identifier: CA032956

Gene: PKP2

Linked Data

• dbSNP Id: rs747470473
• ExAC: 12:32974253 T / C
• gnomAD v2: 12-32974253-T-C
• gnomAD v4: 12-32821319-T-C
• MyVariant Identifiers: chr12:g.32974253T>C (hg19) ; chr12:g.32821319T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32821319T>C , CM000674.2:g.32821319T>C	GRCh38
NC_000012.11:g.32974253T>C , CM000674.1:g.32974253T>C	GRCh37
NC_000012.10:g.32865520T>C	NCBI36
NG_009000.1:g.80528A>G , LRG_398:g.80528A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000700555.2:n.516+37A>G
ENST00000700559.2:c.2013+37A>G	ENSP00000515065.2:n.2013+37A>G
ENST00000700563.2:c.2013+37A>G	ENSP00000515066.2:n.2013+37A>G
ENST00000546498.2:n.700+37A>G
ENST00000549461.2:n.552+37A>G
ENST00000700555.1:c.444+37A>G	ENSP00000515062.1:n.444+37A>G
ENST00000700556.1:c.484+37A>G
ENST00000700558.1:n.227+37A>G
ENST00000700559.1:c.1228+37A>G
ENST00000700560.1:n.1228+37A>G
ENST00000700561.1:n.1354+37A>G
ENST00000700562.1:n.551+37A>G
ENST00000700563.1:c.1967+37A>G
ENST00000700564.1:n.2054A>G
ENST00000070846.11:c.2145+37A>G	ENSP00000070846.6:n.2145+37A>G
ENST00000340811.9:c.2013+37A>G MANE Select	ENSP00000342800.5:n.2013+37A>G
ENST00000070846.10:c.2145+37A>G	ENSP00000070846.6:n.2145+37A>G
ENST00000340811.8:c.2013+37A>G	ENSP00000342800.4:n.2013+37A>G
ENST00000549461.1:n.459+37A>G
ENST00000552612.5:n.471A>G
ENST00000613243.1:c.2145+37A>G	ENSP00000478295.1:n.2145+37A>G
NM_001005242.2:c.2013+37A>G	NP_001005242.2:n.2013+37A>G
NM_004572.3:c.2145+37A>G , LRG_398t1:c.2145+37A>G	NP_004563.2:n.2145+37A>G
NM_001005242.3:c.2013+37A>G MANE Select	NP_001005242.2:n.2013+37A>G
NM_004572.4:c.2145+37A>G	NP_004563.2:n.2145+37A>G