Canonical Allele Identifier: CA479174996
Gene: PKP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.33031911A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32878977A>G , CM000674.2:g.32878977A>G GRCh38
NC_000012.11:g.33031911A>G , CM000674.1:g.33031911A>G GRCh37
NC_000012.10:g.32923178A>G NCBI36
NG_009000.1:g.22870T>C , LRG_398:g.22870T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700559.2:c.279T>C ENSP00000515065.2:p.Val93=
ENST00000700563.2:c.279T>C ENSP00000515066.2:p.Val93=
ENST00000700563.1:c.233T>C
ENST00000700564.1:n.283T>C
ENST00000700565.1:n.132T>C
ENST00000070846.11:c.279T>C ENSP00000070846.6:p.Val93=
ENST00000340811.9:c.279T>C MANE Select ENSP00000342800.5:p.Val93=
ENST00000070846.10:c.279T>C ENSP00000070846.6:p.Val93=
ENST00000340811.8:c.279T>C ENSP00000342800.4:p.Val93=
ENST00000613243.1:c.279T>C ENSP00000478295.1:p.Val93=
NM_001005242.2:c.279T>C NP_001005242.2:p.Val93=
NM_004572.3:c.279T>C , LRG_398t1:c.279T>C NP_004563.2:p.Val93=
NM_001005242.3:c.279T>C MANE Select NP_001005242.2:p.Val93=
NM_004572.4:c.279T>C NP_004563.2:p.Val93=