Canonical Allele Identifier: CA011995

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32796206T>C , CM000674.2:g.32796206T>C	GRCh38
NC_000012.11:g.32949140T>C , CM000674.1:g.32949140T>C	GRCh37
NC_000012.10:g.32840407T>C	NCBI36
NG_009000.1:g.105641A>G , LRG_398:g.105641A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.763A>G
ENST00000700557.2:n.352A>G
ENST00000700559.2:c.2168-3475A>G	ENSP00000515065.2:n.2168-3475A>G
ENST00000546498.2:n.947A>G
ENST00000549461.2:n.752A>G
ENST00000700555.1:c.691A>G	ENSP00000515062.1:p.Thr231Ala
ENST00000700556.1:c.731A>G
ENST00000700557.1:c.271A>G	ENSP00000515064.1:p.Thr91Ala
ENST00000700558.1:n.474A>G
ENST00000700559.1:c.1383-3475A>G
ENST00000700560.1:n.1475A>G
ENST00000700561.1:n.1601A>G
ENST00000070846.11:c.2392A>G	ENSP00000070846.6:p.Thr798Ala
ENST00000340811.9:c.2260A>G MANE Select	ENSP00000342800.5:p.Thr754Ala
ENST00000070846.10:c.2392A>G	ENSP00000070846.6:p.Thr798Ala
ENST00000340811.8:c.2260A>G	ENSP00000342800.4:p.Thr754Ala
ENST00000613243.1:c.2392A>G	ENSP00000478295.1:p.Thr798Ala
NM_001005242.2:c.2260A>G	NP_001005242.2:p.Thr754Ala
NM_004572.3:c.2392A>G , LRG_398t1:c.2392A>G	NP_004563.2:p.Thr798Ala
NM_001005242.3:c.2260A>G MANE Select	NP_001005242.2:p.Thr754Ala
NM_004572.4:c.2392A>G	NP_004563.2:p.Thr798Ala