Canonical Allele Identifier: CA2026396373

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32821491G= , CM000674.2:g.32821491G=	GRCh38
NC_000012.11:g.32974425G= , CM000674.1:g.32974425G=	GRCh37
NC_000012.10:g.32865692G=	NCBI36
NG_009000.1:g.80356C= , LRG_398:g.80356C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.381C=
ENST00000700559.2:c.1878C=	ENSP00000515065.2:p.Asn626=
ENST00000700563.2:c.1878C=	ENSP00000515066.2:p.Asn626=
ENST00000546498.2:n.565C=
ENST00000549461.2:n.417C=
ENST00000700555.1:c.309C=	ENSP00000515062.1:p.Asn103=
ENST00000700556.1:c.349C=
ENST00000700558.1:n.92C=
ENST00000700559.1:c.1093C=
ENST00000700560.1:n.1093C=
ENST00000700561.1:n.1219C=
ENST00000700562.1:n.416C=
ENST00000700563.1:c.1832C=
ENST00000700564.1:n.1882C=
ENST00000070846.11:c.2010C=	ENSP00000070846.6:p.Asn670=
ENST00000340811.9:c.1878C= MANE Select	ENSP00000342800.5:p.Asn626=
ENST00000070846.10:c.2010C=	ENSP00000070846.6:p.Asn670=
ENST00000340811.8:c.1878C=	ENSP00000342800.4:p.Asn626=
ENST00000546498.1:n.565C=
ENST00000549461.1:n.324C=
ENST00000552612.5:n.299C=
ENST00000613243.1:c.2010C=	ENSP00000478295.1:p.Asn670=
NM_001005242.2:c.1878C=	NP_001005242.2:p.Asn626=
NM_004572.3:c.2010C= , LRG_398t1:c.2010C=	NP_004563.2:p.Asn670=
NM_001005242.3:c.1878C= MANE Select	NP_001005242.2:p.Asn626=
NM_004572.4:c.2010C=	NP_004563.2:p.Asn670=