Canonical Allele Identifier: CA2026374161
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32802462T= , CM000674.2:g.32802462T= GRCh38
NC_000012.11:g.32955396T= , CM000674.1:g.32955396T= GRCh37
NC_000012.10:g.32846663T= NCBI36
NG_009000.1:g.99385A= , LRG_398:g.99385A=

Transcript Alleles

HGVS Amino-acid change
ENST00000700555.2:n.611A=
ENST00000700557.2:n.200A=
ENST00000700559.2:c.2108A= ENSP00000515065.2:p.Lys703=
ENST00000546498.2:n.795A=
ENST00000549461.2:n.647A=
ENST00000700555.1:c.539A= ENSP00000515062.1:p.Lys180=
ENST00000700556.1:c.579A=
ENST00000700557.1:c.119A= ENSP00000515064.1:p.Lys40=
ENST00000700558.1:n.322A=
ENST00000700559.1:c.1323A=
ENST00000700560.1:n.1323A=
ENST00000700561.1:n.1449A=
ENST00000070846.11:c.2240A= ENSP00000070846.6:p.Lys747=
ENST00000340811.9:c.2108A= MANE Select ENSP00000342800.5:p.Lys703=
ENST00000070846.10:c.2240A= ENSP00000070846.6:p.Lys747=
ENST00000340811.8:c.2108A= ENSP00000342800.4:p.Lys703=
ENST00000549461.1:n.554A=
ENST00000613243.1:c.2240A= ENSP00000478295.1:p.Lys747=
NM_001005242.2:c.2108A= NP_001005242.2:p.Lys703=
NM_004572.3:c.2240A= , LRG_398t1:c.2240A= NP_004563.2:p.Lys747=
NM_001005242.3:c.2108A= MANE Select NP_001005242.2:p.Lys703=
NM_004572.4:c.2240A= NP_004563.2:p.Lys747=