Canonical Allele Identifier: CA2618225581
Gene: PKP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32822716T>C , CM000674.2:g.32822716T>C GRCh38
NC_000012.11:g.32975650T>C , CM000674.1:g.32975650T>C GRCh37
NC_000012.10:g.32866917T>C NCBI36
NG_009000.1:g.79131A>G , LRG_398:g.79131A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.187-85A>G
ENST00000700559.2:c.1675-85A>G ENSP00000515065.2:n.1675-85A>G
ENST00000700563.2:c.1675-85A>G ENSP00000515066.2:n.1675-85A>G
ENST00000546498.2:n.362-85A>G
ENST00000700555.1:c.115-85A>G ENSP00000515062.1:n.115-85A>G
ENST00000700556.1:c.146-85A>G
ENST00000700559.1:c.890-85A>G
ENST00000700560.1:n.890-85A>G
ENST00000700561.1:n.1016-85A>G
ENST00000700563.1:c.1629-85A>G
ENST00000700564.1:n.1679-85A>G
ENST00000070846.11:c.1807-85A>G ENSP00000070846.6:n.1807-85A>G
ENST00000340811.9:c.1675-85A>G MANE Select ENSP00000342800.5:n.1675-85A>G
ENST00000070846.10:c.1807-85A>G ENSP00000070846.6:n.1807-85A>G
ENST00000340811.8:c.1675-85A>G ENSP00000342800.4:n.1675-85A>G
ENST00000546498.1:n.362-85A>G
ENST00000552612.5:n.96-85A>G
ENST00000613243.1:c.1807-85A>G ENSP00000478295.1:n.1807-85A>G
NM_001005242.2:c.1675-85A>G NP_001005242.2:n.1675-85A>G
NM_004572.3:c.1807-85A>G , LRG_398t1:c.1807-85A>G NP_004563.2:n.1807-85A>G
NM_001005242.3:c.1675-85A>G MANE Select NP_001005242.2:n.1675-85A>G
NM_004572.4:c.1807-85A>G NP_004563.2:n.1807-85A>G