Canonical Allele Identifier: CA2026396039
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32821324T= , CM000674.2:g.32821324T= GRCh38
NC_000012.11:g.32974258T= , CM000674.1:g.32974258T= GRCh37
NC_000012.10:g.32865525T= NCBI36
NG_009000.1:g.80523A= , LRG_398:g.80523A=

Transcript Alleles

HGVS Amino-acid change
ENST00000700555.2:n.516+32A=
ENST00000700559.2:c.2013+32A= ENSP00000515065.2:n.2013+32A=
ENST00000700563.2:c.2013+32A= ENSP00000515066.2:n.2013+32A=
ENST00000546498.2:n.700+32A=
ENST00000549461.2:n.552+32A=
ENST00000700555.1:c.444+32A= ENSP00000515062.1:n.444+32A=
ENST00000700556.1:c.484+32A=
ENST00000700558.1:n.227+32A=
ENST00000700559.1:c.1228+32A=
ENST00000700560.1:n.1228+32A=
ENST00000700561.1:n.1354+32A=
ENST00000700562.1:n.551+32A=
ENST00000700563.1:c.1967+32A=
ENST00000700564.1:n.2049A=
ENST00000070846.11:c.2145+32A= ENSP00000070846.6:n.2145+32A=
ENST00000340811.9:c.2013+32A= MANE Select ENSP00000342800.5:n.2013+32A=
ENST00000070846.10:c.2145+32A= ENSP00000070846.6:n.2145+32A=
ENST00000340811.8:c.2013+32A= ENSP00000342800.4:n.2013+32A=
ENST00000549461.1:n.459+32A=
ENST00000552612.5:n.466A=
ENST00000613243.1:c.2145+32A= ENSP00000478295.1:n.2145+32A=
NM_001005242.2:c.2013+32A= NP_001005242.2:n.2013+32A=
NM_004572.3:c.2145+32A= , LRG_398t1:c.2145+32A= NP_004563.2:n.2145+32A=
NM_001005242.3:c.2013+32A= MANE Select NP_001005242.2:n.2013+32A=
NM_004572.4:c.2145+32A= NP_004563.2:n.2145+32A=