Canonical Allele Identifier: CA2026396192
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32821406G= , CM000674.2:g.32821406G= GRCh38
NC_000012.11:g.32974340G= , CM000674.1:g.32974340G= GRCh37
NC_000012.10:g.32865607G= NCBI36
NG_009000.1:g.80441C= , LRG_398:g.80441C=

Transcript Alleles

HGVS Amino-acid change
ENST00000700555.2:n.466C=
ENST00000700559.2:c.1963C= ENSP00000515065.2:p.Gln655=
ENST00000700563.2:c.1963C= ENSP00000515066.2:p.Gln655=
ENST00000546498.2:n.650C=
ENST00000549461.2:n.502C=
ENST00000700555.1:c.394C= ENSP00000515062.1:p.Gln132=
ENST00000700556.1:c.434C=
ENST00000700558.1:n.177C=
ENST00000700559.1:c.1178C=
ENST00000700560.1:n.1178C=
ENST00000700561.1:n.1304C=
ENST00000700562.1:n.501C=
ENST00000700563.1:c.1917C=
ENST00000700564.1:n.1967C=
ENST00000070846.11:c.2095C= ENSP00000070846.6:p.Gln699=
ENST00000340811.9:c.1963C= MANE Select ENSP00000342800.5:p.Gln655=
ENST00000070846.10:c.2095C= ENSP00000070846.6:p.Gln699=
ENST00000340811.8:c.1963C= ENSP00000342800.4:p.Gln655=
ENST00000549461.1:n.409C=
ENST00000552612.5:n.384C=
ENST00000613243.1:c.2095C= ENSP00000478295.1:p.Gln699=
NM_001005242.2:c.1963C= NP_001005242.2:p.Gln655=
NM_004572.3:c.2095C= , LRG_398t1:c.2095C= NP_004563.2:p.Gln699=
NM_001005242.3:c.1963C= MANE Select NP_001005242.2:p.Gln655=
NM_004572.4:c.2095C= NP_004563.2:p.Gln699=