Canonical Allele Identifier: CA2618226823

Gene: PKP2

Linked Data

• gnomAD v4: 12-32878916-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32878916C>A , CM000674.2:g.32878916C>A	GRCh38
NC_000012.11:g.33031850C>A , CM000674.1:g.33031850C>A	GRCh37
NC_000012.10:g.32923117C>A	NCBI36
NG_009000.1:g.22931G>T , LRG_398:g.22931G>T

Transcript Alleles

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