Canonical Allele Identifier: CA2618224638
Gene: PKP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32821331G>C , CM000674.2:g.32821331G>C GRCh38
NC_000012.11:g.32974265G>C , CM000674.1:g.32974265G>C GRCh37
NC_000012.10:g.32865532G>C NCBI36
NG_009000.1:g.80516C>G , LRG_398:g.80516C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000700555.2:n.516+25C>G
ENST00000700559.2:c.2013+25C>G ENSP00000515065.2:n.2013+25C>G
ENST00000700563.2:c.2013+25C>G ENSP00000515066.2:n.2013+25C>G
ENST00000546498.2:n.700+25C>G
ENST00000549461.2:n.552+25C>G
ENST00000700555.1:c.444+25C>G ENSP00000515062.1:n.444+25C>G
ENST00000700556.1:c.484+25C>G
ENST00000700558.1:n.227+25C>G
ENST00000700559.1:c.1228+25C>G
ENST00000700560.1:n.1228+25C>G
ENST00000700561.1:n.1354+25C>G
ENST00000700562.1:n.551+25C>G
ENST00000700563.1:c.1967+25C>G
ENST00000700564.1:n.2042C>G
ENST00000070846.11:c.2145+25C>G ENSP00000070846.6:n.2145+25C>G
ENST00000340811.9:c.2013+25C>G MANE Select ENSP00000342800.5:n.2013+25C>G
ENST00000070846.10:c.2145+25C>G ENSP00000070846.6:n.2145+25C>G
ENST00000340811.8:c.2013+25C>G ENSP00000342800.4:n.2013+25C>G
ENST00000549461.1:n.459+25C>G
ENST00000552612.5:n.459C>G
ENST00000613243.1:c.2145+25C>G ENSP00000478295.1:n.2145+25C>G
NM_001005242.2:c.2013+25C>G NP_001005242.2:n.2013+25C>G
NM_004572.3:c.2145+25C>G , LRG_398t1:c.2145+25C>G NP_004563.2:n.2145+25C>G
NM_001005242.3:c.2013+25C>G MANE Select NP_001005242.2:n.2013+25C>G
NM_004572.4:c.2145+25C>G NP_004563.2:n.2145+25C>G