Canonical Allele Identifier: CA384357791
Gene: PKP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32796208T>A , CM000674.2:g.32796208T>A GRCh38
NC_000012.11:g.32949142T>A , CM000674.1:g.32949142T>A GRCh37
NC_000012.10:g.32840409T>A NCBI36
NG_009000.1:g.105639A>T , LRG_398:g.105639A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.761A>T
ENST00000700557.2:n.350A>T
ENST00000700559.2:c.2168-3477A>T ENSP00000515065.2:n.2168-3477A>T
ENST00000546498.2:n.945A>T
ENST00000549461.2:n.750A>T
ENST00000700555.1:c.689A>T ENSP00000515062.1:p.Tyr230Phe
ENST00000700556.1:c.729A>T
ENST00000700557.1:c.269A>T ENSP00000515064.1:p.Tyr90Phe
ENST00000700558.1:n.472A>T
ENST00000700559.1:c.1383-3477A>T
ENST00000700560.1:n.1473A>T
ENST00000700561.1:n.1599A>T
ENST00000070846.11:c.2390A>T ENSP00000070846.6:p.Tyr797Phe
ENST00000340811.9:c.2258A>T MANE Select ENSP00000342800.5:p.Tyr753Phe
ENST00000070846.10:c.2390A>T ENSP00000070846.6:p.Tyr797Phe
ENST00000340811.8:c.2258A>T ENSP00000342800.4:p.Tyr753Phe
ENST00000613243.1:c.2390A>T ENSP00000478295.1:p.Tyr797Phe
NM_001005242.2:c.2258A>T NP_001005242.2:p.Tyr753Phe
NM_004572.3:c.2390A>T , LRG_398t1:c.2390A>T NP_004563.2:p.Tyr797Phe
NM_001005242.3:c.2258A>T MANE Select NP_001005242.2:p.Tyr753Phe
NM_004572.4:c.2390A>T NP_004563.2:p.Tyr797Phe