Canonical Allele Identifier: CA2026355546

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32792494T= , CM000674.2:g.32792494T=	GRCh38
NC_000012.11:g.32945428T= , CM000674.1:g.32945428T=	GRCh37
NC_000012.10:g.32836695T=	NCBI36
NG_009000.1:g.109353A= , LRG_398:g.109353A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001005242.3:c.2446-2A= MANE Select	NP_001005242.2:n.2446-2A=
ENST00000340811.9:c.2446-2A= MANE Select	ENSP00000342800.5:n.2446-2A=
NM_001005242.2:c.2446-2A=	NP_001005242.2:n.2446-2A=
NM_004572.3:c.2578-2A= , LRG_398t1:c.2578-2A=	NP_004563.2:n.2578-2A=
NM_004572.4:c.2578-2A=	NP_004563.2:n.2578-2A=
ENST00000070846.10:c.2578-2A=	ENSP00000070846.6:n.2578-2A=
ENST00000070846.11:c.2578-2A=	ENSP00000070846.6:n.2578-2A=
ENST00000340811.8:c.2446-2A=	ENSP00000342800.4:n.2446-2A=
ENST00000546498.2:n.1133-2A=
ENST00000546769.1:n.233-2A=
ENST00000549461.2:n.938-2A=
ENST00000613243.1:c.2576-2A=	ENSP00000478295.1:n.2576-2A=
ENST00000700555.1:c.877-2A=	ENSP00000515062.1:n.877-2A=
ENST00000700555.2:n.949-2A=
ENST00000700556.1:c.917-2A=
ENST00000700557.1:c.457-2A=	ENSP00000515064.1:n.457-2A=
ENST00000700557.2:n.538-2A=
ENST00000700558.1:n.660-2A=
ENST00000700559.1:c.1471-2A=
ENST00000700559.2:c.2256-2A=	ENSP00000515065.2:n.2256-2A=
ENST00000700560.1:n.1810A=