Canonical Allele Identifier: CA036731

Gene: PKP2

Linked Data

• dbSNP Id: rs763552498
• ExAC: 12:33031832 G / A
• gnomAD v2: 12-33031832-G-A
• gnomAD v4: 12-32878898-G-A
• MyVariant Identifiers: chr12:g.33031832G>A (hg19) ; chr12:g.32878898G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32878898G>A , CM000674.2:g.32878898G>A	GRCh38
NC_000012.11:g.33031832G>A , CM000674.1:g.33031832G>A	GRCh37
NC_000012.10:g.32923099G>A	NCBI36
NG_009000.1:g.22949C>T , LRG_398:g.22949C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700559.2:c.336+22C>T	ENSP00000515065.2:n.336+22C>T
ENST00000700563.2:c.336+22C>T	ENSP00000515066.2:n.336+22C>T
ENST00000700563.1:c.290+22C>T
ENST00000700564.1:n.340+22C>T
ENST00000700565.1:n.189+22C>T
ENST00000070846.11:c.336+22C>T	ENSP00000070846.6:n.336+22C>T
ENST00000340811.9:c.336+22C>T MANE Select	ENSP00000342800.5:n.336+22C>T
ENST00000070846.10:c.336+22C>T	ENSP00000070846.6:n.336+22C>T
ENST00000340811.8:c.336+22C>T	ENSP00000342800.4:n.336+22C>T
ENST00000613243.1:c.336+22C>T	ENSP00000478295.1:n.336+22C>T
NM_001005242.2:c.336+22C>T	NP_001005242.2:n.336+22C>T
NM_004572.3:c.336+22C>T , LRG_398t1:c.336+22C>T	NP_004563.2:n.336+22C>T
NM_001005242.3:c.336+22C>T MANE Select	NP_001005242.2:n.336+22C>T
NM_004572.4:c.336+22C>T	NP_004563.2:n.336+22C>T