Canonical Allele Identifier: CA2026396958
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32822510T= , CM000674.2:g.32822510T= GRCh38
NC_000012.11:g.32975444T= , CM000674.1:g.32975444T= GRCh37
NC_000012.10:g.32866711T= NCBI36
NG_009000.1:g.79337A= , LRG_398:g.79337A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.308A=
ENST00000700559.2:c.1796A= ENSP00000515065.2:p.Lys599=
ENST00000700563.2:c.1796A= ENSP00000515066.2:p.Lys599=
ENST00000546498.2:n.483A=
ENST00000700555.1:c.236A= ENSP00000515062.1:p.Lys79=
ENST00000700556.1:c.267A=
ENST00000700559.1:c.1011A=
ENST00000700560.1:n.1011A=
ENST00000700561.1:n.1137A=
ENST00000700563.1:c.1750A=
ENST00000700564.1:n.1800A=
ENST00000070846.11:c.1928A= ENSP00000070846.6:p.Lys643=
ENST00000340811.9:c.1796A= MANE Select ENSP00000342800.5:p.Lys599=
ENST00000070846.10:c.1928A= ENSP00000070846.6:p.Lys643=
ENST00000340811.8:c.1796A= ENSP00000342800.4:p.Lys599=
ENST00000546498.1:n.483A=
ENST00000552612.5:n.217A=
ENST00000613243.1:c.1928A= ENSP00000478295.1:p.Lys643=
NM_001005242.2:c.1796A= NP_001005242.2:p.Lys599=
NM_004572.3:c.1928A= , LRG_398t1:c.1928A= NP_004563.2:p.Lys643=
NM_001005242.3:c.1796A= MANE Select NP_001005242.2:p.Lys599=
NM_004572.4:c.1928A= NP_004563.2:p.Lys643=