Canonical Allele Identifier: CA2026398749

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32824166T= , CM000674.2:g.32824166T=	GRCh38
NC_000012.11:g.32977100T= , CM000674.1:g.32977100T=	GRCh37
NC_000012.10:g.32868367T=	NCBI36
NG_009000.1:g.77681A= , LRG_398:g.77681A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.69-4A=
ENST00000700559.2:c.1557-4A=	ENSP00000515065.2:n.1557-4A=
ENST00000700563.2:c.1557-4A=	ENSP00000515066.2:n.1557-4A=
ENST00000546498.2:n.240A=
ENST00000700555.1:c.-4-4A=	ENSP00000515062.1:n.-4-4A=
ENST00000700556.1:c.28-4A=
ENST00000700559.1:c.772-4A=
ENST00000700560.1:n.772-4A=
ENST00000700561.1:n.898-4A=
ENST00000700563.1:c.1511-4A=
ENST00000700564.1:n.1561-4A=
ENST00000070846.11:c.1689-4A=	ENSP00000070846.6:n.1689-4A=
ENST00000340811.9:c.1557-4A= MANE Select	ENSP00000342800.5:n.1557-4A=
ENST00000070846.10:c.1689-4A=	ENSP00000070846.6:n.1689-4A=
ENST00000340811.8:c.1557-4A=	ENSP00000342800.4:n.1557-4A=
ENST00000546498.1:n.240A=
ENST00000613243.1:c.1689-4A=	ENSP00000478295.1:n.1689-4A=
NM_001005242.2:c.1557-4A=	NP_001005242.2:n.1557-4A=
NM_004572.3:c.1689-4A= , LRG_398t1:c.1689-4A=	NP_004563.2:n.1689-4A=
NM_001005242.3:c.1557-4A= MANE Select	NP_001005242.2:n.1557-4A=
NM_004572.4:c.1689-4A=	NP_004563.2:n.1689-4A=