Canonical Allele Identifier: CA2026373116

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32841029T= , CM000674.2:g.32841029T=	GRCh38
NC_000012.11:g.32993963T= , CM000674.1:g.32993963T=	GRCh37
NC_000012.10:g.32885230T=	NCBI36
NG_009000.1:g.60818A= , LRG_398:g.60818A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001005242.3:c.1555A= MANE Select	NP_001005242.2:p.Arg519=
ENST00000340811.9:c.1555A= MANE Select	ENSP00000342800.5:p.Arg519=
NM_001005242.2:c.1555A=	NP_001005242.2:p.Arg519=
NM_004572.3:c.1687A= , LRG_398t1:c.1687A=	NP_004563.2:p.Arg563=
NM_004572.4:c.1687A=	NP_004563.2:p.Arg563=
ENST00000070846.10:c.1687A=	ENSP00000070846.6:p.Arg563=
ENST00000070846.11:c.1687A=	ENSP00000070846.6:p.Arg563=
ENST00000340811.8:c.1555A=	ENSP00000342800.4:p.Arg519=
ENST00000613243.1:c.1687A=	ENSP00000478295.1:p.Arg563=
ENST00000700556.1:c.26A=
ENST00000700559.1:c.770A=
ENST00000700559.2:c.1555A=	ENSP00000515065.2:p.Arg519=
ENST00000700560.1:n.770A=
ENST00000700561.1:n.896A=
ENST00000700563.1:c.1509A=
ENST00000700563.2:c.1555A=	ENSP00000515066.2:p.Arg519=
ENST00000700564.1:n.1559A=
ENST00000700565.1:n.1408A=