Canonical Allele Identifier: CA687414790

Gene: PKP2

Linked Data

• dbSNP Id: rs1352358110
• gnomAD v4: 12-32879099-T-A
• MyVariant Identifiers: chr12:g.33032033T>A (hg19) ; chr12:g.32879099T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32879099T>A , CM000674.2:g.32879099T>A	GRCh38
NC_000012.11:g.33032033T>A , CM000674.1:g.33032033T>A	GRCh37
NC_000012.10:g.32923300T>A	NCBI36
NG_009000.1:g.22748A>T , LRG_398:g.22748A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700559.2:c.224-67A>T	ENSP00000515065.2:n.224-67A>T
ENST00000700563.2:c.224-67A>T	ENSP00000515066.2:n.224-67A>T
ENST00000700563.1:c.178-67A>T
ENST00000700564.1:n.228-67A>T
ENST00000700565.1:n.77-67A>T
ENST00000070846.11:c.224-67A>T	ENSP00000070846.6:n.224-67A>T
ENST00000340811.9:c.224-67A>T MANE Select	ENSP00000342800.5:n.224-67A>T
ENST00000070846.10:c.224-67A>T	ENSP00000070846.6:n.224-67A>T
ENST00000340811.8:c.224-67A>T	ENSP00000342800.4:n.224-67A>T
ENST00000613243.1:c.224-67A>T	ENSP00000478295.1:n.224-67A>T
NM_001005242.2:c.224-67A>T	NP_001005242.2:n.224-67A>T
NM_004572.3:c.224-67A>T , LRG_398t1:c.224-67A>T	NP_004563.2:n.224-67A>T
NM_001005242.3:c.224-67A>T MANE Select	NP_001005242.2:n.224-67A>T
NM_004572.4:c.224-67A>T	NP_004563.2:n.224-67A>T