Canonical Allele Identifier: CA2026396250
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32821426T= , CM000674.2:g.32821426T= GRCh38
NC_000012.11:g.32974360T= , CM000674.1:g.32974360T= GRCh37
NC_000012.10:g.32865627T= NCBI36
NG_009000.1:g.80421A= , LRG_398:g.80421A=

Transcript Alleles

HGVS Amino-acid change
ENST00000700555.2:n.446A=
ENST00000700559.2:c.1943A= ENSP00000515065.2:p.Lys648=
ENST00000700563.2:c.1943A= ENSP00000515066.2:p.Lys648=
ENST00000546498.2:n.630A=
ENST00000549461.2:n.482A=
ENST00000700555.1:c.374A= ENSP00000515062.1:p.Lys125=
ENST00000700556.1:c.414A=
ENST00000700558.1:n.157A=
ENST00000700559.1:c.1158A=
ENST00000700560.1:n.1158A=
ENST00000700561.1:n.1284A=
ENST00000700562.1:n.481A=
ENST00000700563.1:c.1897A=
ENST00000700564.1:n.1947A=
ENST00000070846.11:c.2075A= ENSP00000070846.6:p.Lys692=
ENST00000340811.9:c.1943A= MANE Select ENSP00000342800.5:p.Lys648=
ENST00000070846.10:c.2075A= ENSP00000070846.6:p.Lys692=
ENST00000340811.8:c.1943A= ENSP00000342800.4:p.Lys648=
ENST00000549461.1:n.389A=
ENST00000552612.5:n.364A=
ENST00000613243.1:c.2075A= ENSP00000478295.1:p.Lys692=
NM_001005242.2:c.1943A= NP_001005242.2:p.Lys648=
NM_004572.3:c.2075A= , LRG_398t1:c.2075A= NP_004563.2:p.Lys692=
NM_001005242.3:c.1943A= MANE Select NP_001005242.2:p.Lys648=
NM_004572.4:c.2075A= NP_004563.2:p.Lys692=