Canonical Allele Identifier: CA2026396846
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32822387T= , CM000674.2:g.32822387T= GRCh38
NC_000012.11:g.32975321T= , CM000674.1:g.32975321T= GRCh37
NC_000012.10:g.32866588T= NCBI36
NG_009000.1:g.79460A= , LRG_398:g.79460A=

Transcript Alleles

HGVS Amino-acid change
ENST00000700555.2:n.342+89A=
ENST00000700559.2:c.1839+80A= ENSP00000515065.2:n.1839+80A=
ENST00000700563.2:c.1839+80A= ENSP00000515066.2:n.1839+80A=
ENST00000546498.2:n.526+80A=
ENST00000700555.1:c.270+89A= ENSP00000515062.1:n.270+89A=
ENST00000700556.1:c.310+80A=
ENST00000700559.1:c.1054+80A=
ENST00000700560.1:n.1054+80A=
ENST00000700561.1:n.1180+80A=
ENST00000700563.1:c.1793+80A=
ENST00000700564.1:n.1843+80A=
ENST00000070846.11:c.1971+80A= ENSP00000070846.6:n.1971+80A=
ENST00000340811.9:c.1839+80A= MANE Select ENSP00000342800.5:n.1839+80A=
ENST00000070846.10:c.1971+80A= ENSP00000070846.6:n.1971+80A=
ENST00000340811.8:c.1839+80A= ENSP00000342800.4:n.1839+80A=
ENST00000546498.1:n.526+80A=
ENST00000552612.5:n.260+80A=
ENST00000613243.1:c.1971+80A= ENSP00000478295.1:n.1971+80A=
NM_001005242.2:c.1839+80A= NP_001005242.2:n.1839+80A=
NM_004572.3:c.1971+80A= , LRG_398t1:c.1971+80A= NP_004563.2:n.1971+80A=
NM_001005242.3:c.1839+80A= MANE Select NP_001005242.2:n.1839+80A=
NM_004572.4:c.1971+80A= NP_004563.2:n.1971+80A=