Canonical Allele Identifier: CA2026360805
Gene: PKP2 HGNC NCBI

Linked Data

dbSNP Id: rs1592726486

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32796321A>C , CM000674.2:g.32796321A>C GRCh38
NC_000012.11:g.32949255A>C , CM000674.1:g.32949255A>C GRCh37
NC_000012.10:g.32840522A>C NCBI36
NG_009000.1:g.105526T>G , LRG_398:g.105526T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.671-23T>G
ENST00000700557.2:n.260-23T>G
ENST00000700559.2:c.2168-3590T>G ENSP00000515065.2:n.2168-3590T>G
ENST00000546498.2:n.855-23T>G
ENST00000549461.2:n.660-23T>G
ENST00000700555.1:c.599-23T>G ENSP00000515062.1:n.599-23T>G
ENST00000700556.1:c.639-23T>G
ENST00000700557.1:c.179-23T>G ENSP00000515064.1:n.179-23T>G
ENST00000700558.1:n.382-23T>G
ENST00000700559.1:c.1383-3590T>G
ENST00000700560.1:n.1383-23T>G
ENST00000700561.1:n.1509-23T>G
ENST00000070846.11:c.2300-23T>G ENSP00000070846.6:n.2300-23T>G
ENST00000340811.9:c.2168-23T>G MANE Select ENSP00000342800.5:n.2168-23T>G
ENST00000070846.10:c.2300-23T>G ENSP00000070846.6:n.2300-23T>G
ENST00000340811.8:c.2168-23T>G ENSP00000342800.4:n.2168-23T>G
ENST00000613243.1:c.2300-23T>G ENSP00000478295.1:n.2300-23T>G
NM_001005242.2:c.2168-23T>G NP_001005242.2:n.2168-23T>G
NM_004572.3:c.2300-23T>G , LRG_398t1:c.2300-23T>G NP_004563.2:n.2300-23T>G
NM_001005242.3:c.2168-23T>G MANE Select NP_001005242.2:n.2168-23T>G
NM_004572.4:c.2300-23T>G NP_004563.2:n.2300-23T>G