Canonical Allele Identifier: CA2026397116

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822616C= , CM000674.2:g.32822616C=	GRCh38
NC_000012.11:g.32975550C= , CM000674.1:g.32975550C=	GRCh37
NC_000012.10:g.32866817C=	NCBI36
NG_009000.1:g.79231G= , LRG_398:g.79231G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.202G=
ENST00000700559.2:c.1690G=	ENSP00000515065.2:p.Val564=
ENST00000700563.2:c.1690G=	ENSP00000515066.2:p.Val564=
ENST00000546498.2:n.377G=
ENST00000700555.1:c.130G=	ENSP00000515062.1:p.Val44=
ENST00000700556.1:c.161G=
ENST00000700559.1:c.905G=
ENST00000700560.1:n.905G=
ENST00000700561.1:n.1031G=
ENST00000700563.1:c.1644G=
ENST00000700564.1:n.1694G=
ENST00000070846.11:c.1822G=	ENSP00000070846.6:p.Val608=
ENST00000340811.9:c.1690G= MANE Select	ENSP00000342800.5:p.Val564=
ENST00000070846.10:c.1822G=	ENSP00000070846.6:p.Val608=
ENST00000340811.8:c.1690G=	ENSP00000342800.4:p.Val564=
ENST00000546498.1:n.377G=
ENST00000552612.5:n.111G=
ENST00000613243.1:c.1822G=	ENSP00000478295.1:p.Val608=
NM_001005242.2:c.1690G=	NP_001005242.2:p.Val564=
NM_004572.3:c.1822G= , LRG_398t1:c.1822G=	NP_004563.2:p.Val608=
NM_001005242.3:c.1690G= MANE Select	NP_001005242.2:p.Val564=
NM_004572.4:c.1822G=	NP_004563.2:p.Val608=