Canonical Allele Identifier: CA2026360480
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32796272A= , CM000674.2:g.32796272A= GRCh38
NC_000012.11:g.32949206A= , CM000674.1:g.32949206A= GRCh37
NC_000012.10:g.32840473A= NCBI36
NG_009000.1:g.105575T= , LRG_398:g.105575T=

Transcript Alleles

HGVS Amino-acid change
ENST00000700555.2:n.697T=
ENST00000700557.2:n.286T=
ENST00000700559.2:c.2168-3541T= ENSP00000515065.2:n.2168-3541T=
ENST00000546498.2:n.881T=
ENST00000549461.2:n.686T=
ENST00000700555.1:c.625T= ENSP00000515062.1:p.Ser209=
ENST00000700556.1:c.665T=
ENST00000700557.1:c.205T= ENSP00000515064.1:p.Ser69=
ENST00000700558.1:n.408T=
ENST00000700559.1:c.1383-3541T=
ENST00000700560.1:n.1409T=
ENST00000700561.1:n.1535T=
ENST00000070846.11:c.2326T= ENSP00000070846.6:p.Ser776=
ENST00000340811.9:c.2194T= MANE Select ENSP00000342800.5:p.Ser732=
ENST00000070846.10:c.2326T= ENSP00000070846.6:p.Ser776=
ENST00000340811.8:c.2194T= ENSP00000342800.4:p.Ser732=
ENST00000613243.1:c.2326T= ENSP00000478295.1:p.Ser776=
NM_001005242.2:c.2194T= NP_001005242.2:p.Ser732=
NM_004572.3:c.2326T= , LRG_398t1:c.2326T= NP_004563.2:p.Ser776=
NM_001005242.3:c.2194T= MANE Select NP_001005242.2:p.Ser732=
NM_004572.4:c.2326T= NP_004563.2:p.Ser776=