Canonical Allele Identifier: CA2026342973

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32869076C= , CM000674.2:g.32869076C=	GRCh38
NC_000012.11:g.33022010C= , CM000674.1:g.33022010C=	GRCh37
NC_000012.10:g.32913277C=	NCBI36
NG_009000.1:g.32771G= , LRG_398:g.32771G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700559.2:c.1035-14G=	ENSP00000515065.2:n.1035-14G=
ENST00000700563.2:c.1035-14G=	ENSP00000515066.2:n.1035-14G=
ENST00000700559.1:c.250-14G=
ENST00000700560.1:n.250-14G=
ENST00000700561.1:n.376-14G=
ENST00000700563.1:c.989-14G=
ENST00000700564.1:n.1039-14G=
ENST00000700565.1:n.888-14G=
ENST00000070846.11:c.1035-14G=	ENSP00000070846.6:n.1035-14G=
ENST00000340811.9:c.1035-14G= MANE Select	ENSP00000342800.5:n.1035-14G=
ENST00000070846.10:c.1035-14G=	ENSP00000070846.6:n.1035-14G=
ENST00000340811.8:c.1035-14G=	ENSP00000342800.4:n.1035-14G=
ENST00000613243.1:c.1035-14G=	ENSP00000478295.1:n.1035-14G=
NM_001005242.2:c.1035-14G=	NP_001005242.2:n.1035-14G=
NM_004572.3:c.1035-14G= , LRG_398t1:c.1035-14G=	NP_004563.2:n.1035-14G=
NM_001005242.3:c.1035-14G= MANE Select	NP_001005242.2:n.1035-14G=
NM_004572.4:c.1035-14G=	NP_004563.2:n.1035-14G=