Canonical Allele Identifier: CA2026374472

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32802542C= , CM000674.2:g.32802542C=	GRCh38
NC_000012.11:g.32955476C= , CM000674.1:g.32955476C=	GRCh37
NC_000012.10:g.32846743C=	NCBI36
NG_009000.1:g.99305G= , LRG_398:g.99305G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.531G=
ENST00000700557.2:n.120G=
ENST00000700559.2:c.2028G=	ENSP00000515065.2:p.Val676=
ENST00000546498.2:n.715G=
ENST00000549461.2:n.567G=
ENST00000700555.1:c.459G=	ENSP00000515062.1:p.Val153=
ENST00000700556.1:c.499G=
ENST00000700557.1:c.39G=	ENSP00000515064.1:p.Val13=
ENST00000700558.1:n.242G=
ENST00000700559.1:c.1243G=
ENST00000700560.1:n.1243G=
ENST00000700561.1:n.1369G=
ENST00000070846.11:c.2160G=	ENSP00000070846.6:p.Val720=
ENST00000340811.9:c.2028G= MANE Select	ENSP00000342800.5:p.Val676=
ENST00000070846.10:c.2160G=	ENSP00000070846.6:p.Val720=
ENST00000340811.8:c.2028G=	ENSP00000342800.4:p.Val676=
ENST00000549461.1:n.474G=
ENST00000613243.1:c.2160G=	ENSP00000478295.1:p.Val720=
NM_001005242.2:c.2028G=	NP_001005242.2:p.Val676=
NM_004572.3:c.2160G= , LRG_398t1:c.2160G=	NP_004563.2:p.Val720=
NM_001005242.3:c.2028G= MANE Select	NP_001005242.2:p.Val676=
NM_004572.4:c.2160G=	NP_004563.2:p.Val720=