Canonical Allele Identifier: CA2026397217
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32822701A= , CM000674.2:g.32822701A= GRCh38
NC_000012.11:g.32975635A= , CM000674.1:g.32975635A= GRCh37
NC_000012.10:g.32866902A= NCBI36
NG_009000.1:g.79146T= , LRG_398:g.79146T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.187-70T=
ENST00000700559.2:c.1675-70T= ENSP00000515065.2:n.1675-70T=
ENST00000700563.2:c.1675-70T= ENSP00000515066.2:n.1675-70T=
ENST00000546498.2:n.362-70T=
ENST00000700555.1:c.115-70T= ENSP00000515062.1:n.115-70T=
ENST00000700556.1:c.146-70T=
ENST00000700559.1:c.890-70T=
ENST00000700560.1:n.890-70T=
ENST00000700561.1:n.1016-70T=
ENST00000700563.1:c.1629-70T=
ENST00000700564.1:n.1679-70T=
ENST00000070846.11:c.1807-70T= ENSP00000070846.6:n.1807-70T=
ENST00000340811.9:c.1675-70T= MANE Select ENSP00000342800.5:n.1675-70T=
ENST00000070846.10:c.1807-70T= ENSP00000070846.6:n.1807-70T=
ENST00000340811.8:c.1675-70T= ENSP00000342800.4:n.1675-70T=
ENST00000546498.1:n.362-70T=
ENST00000552612.5:n.96-70T=
ENST00000613243.1:c.1807-70T= ENSP00000478295.1:n.1807-70T=
NM_001005242.2:c.1675-70T= NP_001005242.2:n.1675-70T=
NM_004572.3:c.1807-70T= , LRG_398t1:c.1807-70T= NP_004563.2:n.1807-70T=
NM_001005242.3:c.1675-70T= MANE Select NP_001005242.2:n.1675-70T=
NM_004572.4:c.1807-70T= NP_004563.2:n.1807-70T=