Canonical Allele Identifier: CA2026374150
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32802457C= , CM000674.2:g.32802457C= GRCh38
NC_000012.11:g.32955391C= , CM000674.1:g.32955391C= GRCh37
NC_000012.10:g.32846658C= NCBI36
NG_009000.1:g.99390G= , LRG_398:g.99390G=

Transcript Alleles

HGVS Amino-acid change
ENST00000700555.2:n.616G=
ENST00000700557.2:n.205G=
ENST00000700559.2:c.2113G= ENSP00000515065.2:p.Ala705=
ENST00000546498.2:n.800G=
ENST00000549461.2:n.652G=
ENST00000700555.1:c.544G= ENSP00000515062.1:p.Ala182=
ENST00000700556.1:c.584G=
ENST00000700557.1:c.124G= ENSP00000515064.1:p.Ala42=
ENST00000700558.1:n.327G=
ENST00000700559.1:c.1328G=
ENST00000700560.1:n.1328G=
ENST00000700561.1:n.1454G=
ENST00000070846.11:c.2245G= ENSP00000070846.6:p.Ala749=
ENST00000340811.9:c.2113G= MANE Select ENSP00000342800.5:p.Ala705=
ENST00000070846.10:c.2245G= ENSP00000070846.6:p.Ala749=
ENST00000340811.8:c.2113G= ENSP00000342800.4:p.Ala705=
ENST00000549461.1:n.559G=
ENST00000613243.1:c.2245G= ENSP00000478295.1:p.Ala749=
NM_001005242.2:c.2113G= NP_001005242.2:p.Ala705=
NM_004572.3:c.2245G= , LRG_398t1:c.2245G= NP_004563.2:p.Ala749=
NM_001005242.3:c.2113G= MANE Select NP_001005242.2:p.Ala705=
NM_004572.4:c.2245G= NP_004563.2:p.Ala749=