Canonical Allele Identifier: CA2026350091

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32877900C= , CM000674.2:g.32877900C=	GRCh38
NC_000012.11:g.33030834C= , CM000674.1:g.33030834C=	GRCh37
NC_000012.10:g.32922101C=	NCBI36
NG_009000.1:g.23947G= , LRG_398:g.23947G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700559.2:c.980G=	ENSP00000515065.2:p.Gly327=
ENST00000700563.2:c.980G=	ENSP00000515066.2:p.Gly327=
ENST00000700559.1:c.195G=
ENST00000700560.1:n.195G=
ENST00000700561.1:n.321G=
ENST00000700563.1:c.934G=
ENST00000700564.1:n.984G=
ENST00000700565.1:n.833G=
ENST00000070846.11:c.980G=	ENSP00000070846.6:p.Gly327=
ENST00000340811.9:c.980G= MANE Select	ENSP00000342800.5:p.Gly327=
ENST00000070846.10:c.980G=	ENSP00000070846.6:p.Gly327=
ENST00000340811.8:c.980G=	ENSP00000342800.4:p.Gly327=
ENST00000613243.1:c.980G=	ENSP00000478295.1:p.Gly327=
NM_001005242.2:c.980G=	NP_001005242.2:p.Gly327=
NM_004572.3:c.980G= , LRG_398t1:c.980G=	NP_004563.2:p.Gly327=
NM_001005242.3:c.980G= MANE Select	NP_001005242.2:p.Gly327=
NM_004572.4:c.980G=	NP_004563.2:p.Gly327=