Canonical Allele Identifier: CA384357916
Gene: PKP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32796269T>A , CM000674.2:g.32796269T>A GRCh38
NC_000012.11:g.32949203T>A , CM000674.1:g.32949203T>A GRCh37
NC_000012.10:g.32840470T>A NCBI36
NG_009000.1:g.105578A>T , LRG_398:g.105578A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000700555.2:n.700A>T
ENST00000700557.2:n.289A>T
ENST00000700559.2:c.2168-3538A>T ENSP00000515065.2:n.2168-3538A>T
ENST00000546498.2:n.884A>T
ENST00000549461.2:n.689A>T
ENST00000700555.1:c.628A>T ENSP00000515062.1:p.Ile210Phe
ENST00000700556.1:c.668A>T
ENST00000700557.1:c.208A>T ENSP00000515064.1:p.Ile70Phe
ENST00000700558.1:n.411A>T
ENST00000700559.1:c.1383-3538A>T
ENST00000700560.1:n.1412A>T
ENST00000700561.1:n.1538A>T
ENST00000070846.11:c.2329A>T ENSP00000070846.6:p.Ile777Phe
ENST00000340811.9:c.2197A>T MANE Select ENSP00000342800.5:p.Ile733Phe
ENST00000070846.10:c.2329A>T ENSP00000070846.6:p.Ile777Phe
ENST00000340811.8:c.2197A>T ENSP00000342800.4:p.Ile733Phe
ENST00000613243.1:c.2329A>T ENSP00000478295.1:p.Ile777Phe
NM_001005242.2:c.2197A>T NP_001005242.2:p.Ile733Phe
NM_004572.3:c.2329A>T , LRG_398t1:c.2329A>T NP_004563.2:p.Ile777Phe
NM_001005242.3:c.2197A>T MANE Select NP_001005242.2:p.Ile733Phe
NM_004572.4:c.2329A>T NP_004563.2:p.Ile777Phe