Canonical Allele Identifier: CA2026361471

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32796687C= , CM000674.2:g.32796687C=	GRCh38
NC_000012.11:g.32949621C= , CM000674.1:g.32949621C=	GRCh37
NC_000012.10:g.32840888C=	NCBI36
NG_009000.1:g.105160G= , LRG_398:g.105160G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.671-389G=
ENST00000700557.2:n.260-389G=
ENST00000700559.2:c.2168-3956G=	ENSP00000515065.2:n.2168-3956G=
ENST00000546498.2:n.855-389G=
ENST00000549461.2:n.660-389G=
ENST00000700555.1:c.599-389G=	ENSP00000515062.1:n.599-389G=
ENST00000700556.1:c.639-389G=
ENST00000700557.1:c.179-389G=	ENSP00000515064.1:n.179-389G=
ENST00000700558.1:n.382-389G=
ENST00000700559.1:c.1383-3956G=
ENST00000700560.1:n.1383-389G=
ENST00000700561.1:n.1509-389G=
ENST00000070846.11:c.2300-389G=	ENSP00000070846.6:n.2300-389G=
ENST00000340811.9:c.2168-389G= MANE Select	ENSP00000342800.5:n.2168-389G=
ENST00000070846.10:c.2300-389G=	ENSP00000070846.6:n.2300-389G=
ENST00000340811.8:c.2168-389G=	ENSP00000342800.4:n.2168-389G=
ENST00000613243.1:c.2300-389G=	ENSP00000478295.1:n.2300-389G=
NM_001005242.2:c.2168-389G=	NP_001005242.2:n.2168-389G=
NM_004572.3:c.2300-389G= , LRG_398t1:c.2300-389G=	NP_004563.2:n.2300-389G=
NM_001005242.3:c.2168-389G= MANE Select	NP_001005242.2:n.2168-389G=
NM_004572.4:c.2300-389G=	NP_004563.2:n.2300-389G=