Canonical Allele Identifier: CA2026352606
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32879022G= , CM000674.2:g.32879022G= GRCh38
NC_000012.11:g.33031956G= , CM000674.1:g.33031956G= GRCh37
NC_000012.10:g.32923223G= NCBI36
NG_009000.1:g.22825C= , LRG_398:g.22825C=

Transcript Alleles

HGVS Amino-acid change
ENST00000700559.2:c.234C= ENSP00000515065.2:p.His78=
ENST00000700563.2:c.234C= ENSP00000515066.2:p.His78=
ENST00000700563.1:c.188C=
ENST00000700564.1:n.238C=
ENST00000700565.1:n.87C=
ENST00000070846.11:c.234C= ENSP00000070846.6:p.His78=
ENST00000340811.9:c.234C= MANE Select ENSP00000342800.5:p.His78=
ENST00000070846.10:c.234C= ENSP00000070846.6:p.His78=
ENST00000340811.8:c.234C= ENSP00000342800.4:p.His78=
ENST00000613243.1:c.234C= ENSP00000478295.1:p.His78=
NM_001005242.2:c.234C= NP_001005242.2:p.His78=
NM_004572.3:c.234C= , LRG_398t1:c.234C= NP_004563.2:p.His78=
NM_001005242.3:c.234C= MANE Select NP_001005242.2:p.His78=
NM_004572.4:c.234C= NP_004563.2:p.His78=