Canonical Allele Identifier: CA384357577
Gene: PKP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32796137T>G , CM000674.2:g.32796137T>G GRCh38
NC_000012.11:g.32949071T>G , CM000674.1:g.32949071T>G GRCh37
NC_000012.10:g.32840338T>G NCBI36
NG_009000.1:g.105710A>C , LRG_398:g.105710A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.832A>C
ENST00000700557.2:n.421A>C
ENST00000700559.2:c.2168-3406A>C ENSP00000515065.2:n.2168-3406A>C
ENST00000546498.2:n.1016A>C
ENST00000549461.2:n.821A>C
ENST00000700555.1:c.760A>C ENSP00000515062.1:p.Lys254Gln
ENST00000700556.1:c.800A>C
ENST00000700557.1:c.340A>C ENSP00000515064.1:p.Lys114Gln
ENST00000700558.1:n.543A>C
ENST00000700559.1:c.1383-3406A>C
ENST00000700560.1:n.1544A>C
ENST00000700561.1:n.1670A>C
ENST00000070846.11:c.2461A>C ENSP00000070846.6:p.Lys821Gln
ENST00000340811.9:c.2329A>C MANE Select ENSP00000342800.5:p.Lys777Gln
ENST00000070846.10:c.2461A>C ENSP00000070846.6:p.Lys821Gln
ENST00000340811.8:c.2329A>C ENSP00000342800.4:p.Lys777Gln
ENST00000613243.1:c.2459A>C ENSP00000478295.1:p.Glu820Ala
NM_001005242.2:c.2329A>C NP_001005242.2:p.Lys777Gln
NM_004572.3:c.2461A>C , LRG_398t1:c.2461A>C NP_004563.2:p.Lys821Gln
NM_001005242.3:c.2329A>C MANE Select NP_001005242.2:p.Lys777Gln
NM_004572.4:c.2461A>C NP_004563.2:p.Lys821Gln