Canonical Allele Identifier: CA2795079556
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32879084T>G , CM000674.2:g.32879084T>G GRCh38
NC_000012.11:g.33032018T>G , CM000674.1:g.33032018T>G GRCh37
NC_000012.10:g.32923285T>G NCBI36
NG_009000.1:g.22763A>C , LRG_398:g.22763A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700559.2:c.224-52A>C ENSP00000515065.2:n.224-52A>C
ENST00000700563.2:c.224-52A>C ENSP00000515066.2:n.224-52A>C
ENST00000700563.1:c.178-52A>C
ENST00000700564.1:n.228-52A>C
ENST00000700565.1:n.77-52A>C
ENST00000070846.11:c.224-52A>C ENSP00000070846.6:n.224-52A>C
ENST00000340811.9:c.224-52A>C MANE Select ENSP00000342800.5:n.224-52A>C
ENST00000070846.10:c.224-52A>C ENSP00000070846.6:n.224-52A>C
ENST00000340811.8:c.224-52A>C ENSP00000342800.4:n.224-52A>C
ENST00000613243.1:c.224-52A>C ENSP00000478295.1:n.224-52A>C
NM_001005242.2:c.224-52A>C NP_001005242.2:n.224-52A>C
NM_004572.3:c.224-52A>C , LRG_398t1:c.224-52A>C NP_004563.2:n.224-52A>C
NM_001005242.3:c.224-52A>C MANE Select NP_001005242.2:n.224-52A>C
NM_004572.4:c.224-52A>C NP_004563.2:n.224-52A>C