Canonical Allele Identifier: CA010636

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32841139G>A , CM000674.2:g.32841139G>A	GRCh38
NC_000012.11:g.32994073G>A , CM000674.1:g.32994073G>A	GRCh37
NC_000012.10:g.32885340G>A	NCBI36
NG_009000.1:g.60708C>T , LRG_398:g.60708C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001005242.3:c.1445C>T MANE Select	NP_001005242.2:p.Thr482Met
ENST00000340811.9:c.1445C>T MANE Select	ENSP00000342800.5:p.Thr482Met
NM_001005242.2:c.1445C>T	NP_001005242.2:p.Thr482Met
NM_004572.3:c.1577C>T , LRG_398t1:c.1577C>T	NP_004563.2:p.Thr526Met
NM_004572.4:c.1577C>T	NP_004563.2:p.Thr526Met
ENST00000070846.10:c.1577C>T	ENSP00000070846.6:p.Thr526Met
ENST00000070846.11:c.1577C>T	ENSP00000070846.6:p.Thr526Met
ENST00000340811.8:c.1445C>T	ENSP00000342800.4:p.Thr482Met
ENST00000613243.1:c.1577C>T	ENSP00000478295.1:p.Thr526Met
ENST00000700559.1:c.660C>T
ENST00000700559.2:c.1445C>T	ENSP00000515065.2:p.Thr482Met
ENST00000700560.1:n.660C>T
ENST00000700561.1:n.786C>T
ENST00000700563.1:c.1399C>T
ENST00000700563.2:c.1445C>T	ENSP00000515066.2:p.Thr482Met
ENST00000700564.1:n.1449C>T
ENST00000700565.1:n.1298C>T