Canonical Allele Identifier: CA2026360877

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32796347T= , CM000674.2:g.32796347T=	GRCh38
NC_000012.11:g.32949281T= , CM000674.1:g.32949281T=	GRCh37
NC_000012.10:g.32840548T=	NCBI36
NG_009000.1:g.105500A= , LRG_398:g.105500A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.671-49A=
ENST00000700557.2:n.260-49A=
ENST00000700559.2:c.2168-3616A=	ENSP00000515065.2:n.2168-3616A=
ENST00000546498.2:n.855-49A=
ENST00000549461.2:n.660-49A=
ENST00000700555.1:c.599-49A=	ENSP00000515062.1:n.599-49A=
ENST00000700556.1:c.639-49A=
ENST00000700557.1:c.179-49A=	ENSP00000515064.1:n.179-49A=
ENST00000700558.1:n.382-49A=
ENST00000700559.1:c.1383-3616A=
ENST00000700560.1:n.1383-49A=
ENST00000700561.1:n.1509-49A=
ENST00000070846.11:c.2300-49A=	ENSP00000070846.6:n.2300-49A=
ENST00000340811.9:c.2168-49A= MANE Select	ENSP00000342800.5:n.2168-49A=
ENST00000070846.10:c.2300-49A=	ENSP00000070846.6:n.2300-49A=
ENST00000340811.8:c.2168-49A=	ENSP00000342800.4:n.2168-49A=
ENST00000613243.1:c.2300-49A=	ENSP00000478295.1:n.2300-49A=
NM_001005242.2:c.2168-49A=	NP_001005242.2:n.2168-49A=
NM_004572.3:c.2300-49A= , LRG_398t1:c.2300-49A=	NP_004563.2:n.2300-49A=
NM_001005242.3:c.2168-49A= MANE Select	NP_001005242.2:n.2168-49A=
NM_004572.4:c.2300-49A=	NP_004563.2:n.2300-49A=