Canonical Allele Identifier: CA2026398776
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32824179A= , CM000674.2:g.32824179A= GRCh38
NC_000012.11:g.32977113A= , CM000674.1:g.32977113A= GRCh37
NC_000012.10:g.32868380A= NCBI36
NG_009000.1:g.77668T= , LRG_398:g.77668T=

Transcript Alleles

HGVS Amino-acid change
ENST00000700555.2:n.69-17T=
ENST00000700559.2:c.1557-17T= ENSP00000515065.2:n.1557-17T=
ENST00000700563.2:c.1557-17T= ENSP00000515066.2:n.1557-17T=
ENST00000546498.2:n.227T=
ENST00000700555.1:c.-4-17T= ENSP00000515062.1:n.-4-17T=
ENST00000700556.1:c.28-17T=
ENST00000700559.1:c.772-17T=
ENST00000700560.1:n.772-17T=
ENST00000700561.1:n.898-17T=
ENST00000700563.1:c.1511-17T=
ENST00000700564.1:n.1561-17T=
ENST00000070846.11:c.1689-17T= ENSP00000070846.6:n.1689-17T=
ENST00000340811.9:c.1557-17T= MANE Select ENSP00000342800.5:n.1557-17T=
ENST00000070846.10:c.1689-17T= ENSP00000070846.6:n.1689-17T=
ENST00000340811.8:c.1557-17T= ENSP00000342800.4:n.1557-17T=
ENST00000546498.1:n.227T=
ENST00000613243.1:c.1689-17T= ENSP00000478295.1:n.1689-17T=
NM_001005242.2:c.1557-17T= NP_001005242.2:n.1557-17T=
NM_004572.3:c.1689-17T= , LRG_398t1:c.1689-17T= NP_004563.2:n.1689-17T=
NM_001005242.3:c.1557-17T= MANE Select NP_001005242.2:n.1557-17T=
NM_004572.4:c.1689-17T= NP_004563.2:n.1689-17T=