Canonical Allele Identifier: CA2026396894
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32822470T= , CM000674.2:g.32822470T= GRCh38
NC_000012.11:g.32975404T= , CM000674.1:g.32975404T= GRCh37
NC_000012.10:g.32866671T= NCBI36
NG_009000.1:g.79377A= , LRG_398:g.79377A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.342+6A=
ENST00000700559.2:c.1836A= ENSP00000515065.2:p.Lys612=
ENST00000700563.2:c.1836A= ENSP00000515066.2:p.Lys612=
ENST00000546498.2:n.523A=
ENST00000700555.1:c.270+6A= ENSP00000515062.1:n.270+6A=
ENST00000700556.1:c.307A=
ENST00000700559.1:c.1051A=
ENST00000700560.1:n.1051A=
ENST00000700561.1:n.1177A=
ENST00000700563.1:c.1790A=
ENST00000700564.1:n.1840A=
ENST00000070846.11:c.1968A= ENSP00000070846.6:p.Lys656=
ENST00000340811.9:c.1836A= MANE Select ENSP00000342800.5:p.Lys612=
ENST00000070846.10:c.1968A= ENSP00000070846.6:p.Lys656=
ENST00000340811.8:c.1836A= ENSP00000342800.4:p.Lys612=
ENST00000546498.1:n.523A=
ENST00000552612.5:n.257A=
ENST00000613243.1:c.1968A= ENSP00000478295.1:p.Lys656=
NM_001005242.2:c.1836A= NP_001005242.2:p.Lys612=
NM_004572.3:c.1968A= , LRG_398t1:c.1968A= NP_004563.2:p.Lys656=
NM_001005242.3:c.1836A= MANE Select NP_001005242.2:p.Lys612=
NM_004572.4:c.1968A= NP_004563.2:p.Lys656=