Canonical Allele Identifier: CA2026396965
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32822515G= , CM000674.2:g.32822515G= GRCh38
NC_000012.11:g.32975449G= , CM000674.1:g.32975449G= GRCh37
NC_000012.10:g.32866716G= NCBI36
NG_009000.1:g.79332C= , LRG_398:g.79332C=

Transcript Alleles

HGVS Amino-acid change
ENST00000700555.2:n.303C=
ENST00000700559.2:c.1791C= ENSP00000515065.2:p.Asn597=
ENST00000700563.2:c.1791C= ENSP00000515066.2:p.Asn597=
ENST00000546498.2:n.478C=
ENST00000700555.1:c.231C= ENSP00000515062.1:p.Asn77=
ENST00000700556.1:c.262C=
ENST00000700559.1:c.1006C=
ENST00000700560.1:n.1006C=
ENST00000700561.1:n.1132C=
ENST00000700563.1:c.1745C=
ENST00000700564.1:n.1795C=
ENST00000070846.11:c.1923C= ENSP00000070846.6:p.Asn641=
ENST00000340811.9:c.1791C= MANE Select ENSP00000342800.5:p.Asn597=
ENST00000070846.10:c.1923C= ENSP00000070846.6:p.Asn641=
ENST00000340811.8:c.1791C= ENSP00000342800.4:p.Asn597=
ENST00000546498.1:n.478C=
ENST00000552612.5:n.212C=
ENST00000613243.1:c.1923C= ENSP00000478295.1:p.Asn641=
NM_001005242.2:c.1791C= NP_001005242.2:p.Asn597=
NM_004572.3:c.1923C= , LRG_398t1:c.1923C= NP_004563.2:p.Asn641=
NM_001005242.3:c.1791C= MANE Select NP_001005242.2:p.Asn597=
NM_004572.4:c.1923C= NP_004563.2:p.Asn641=