Canonical Allele Identifier: CA2026374649
Gene: PKP2 HGNC NCBI

Linked Data

dbSNP Id: rs1956193200

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32802615G>C , CM000674.2:g.32802615G>C GRCh38
NC_000012.11:g.32955549G>C , CM000674.1:g.32955549G>C GRCh37
NC_000012.10:g.32846816G>C NCBI36
NG_009000.1:g.99232C>G , LRG_398:g.99232C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.517-59C>G
ENST00000700557.2:n.106-59C>G
ENST00000700559.2:c.2014-59C>G ENSP00000515065.2:n.2014-59C>G
ENST00000546498.2:n.701-59C>G
ENST00000549461.2:n.553-59C>G
ENST00000700555.1:c.445-59C>G ENSP00000515062.1:n.445-59C>G
ENST00000700556.1:c.485-59C>G
ENST00000700557.1:c.25-59C>G ENSP00000515064.1:n.25-59C>G
ENST00000700558.1:n.228-59C>G
ENST00000700559.1:c.1229-59C>G
ENST00000700560.1:n.1229-59C>G
ENST00000700561.1:n.1355-59C>G
ENST00000070846.11:c.2146-59C>G ENSP00000070846.6:n.2146-59C>G
ENST00000340811.9:c.2014-59C>G MANE Select ENSP00000342800.5:n.2014-59C>G
ENST00000070846.10:c.2146-59C>G ENSP00000070846.6:n.2146-59C>G
ENST00000340811.8:c.2014-59C>G ENSP00000342800.4:n.2014-59C>G
ENST00000549461.1:n.460-59C>G
ENST00000613243.1:c.2146-59C>G ENSP00000478295.1:n.2146-59C>G
NM_001005242.2:c.2014-59C>G NP_001005242.2:n.2014-59C>G
NM_004572.3:c.2146-59C>G , LRG_398t1:c.2146-59C>G NP_004563.2:n.2146-59C>G
NM_001005242.3:c.2014-59C>G MANE Select NP_001005242.2:n.2014-59C>G
NM_004572.4:c.2146-59C>G NP_004563.2:n.2146-59C>G