Canonical Allele Identifier: CA2575161997
Gene: PKP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32823999G>T , CM000674.2:g.32823999G>T GRCh38
NC_000012.11:g.32976933G>T , CM000674.1:g.32976933G>T GRCh37
NC_000012.10:g.32868200G>T NCBI36
NG_009000.1:g.77848C>A , LRG_398:g.77848C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.186+46C>A
ENST00000700559.2:c.1674+46C>A ENSP00000515065.2:n.1674+46C>A
ENST00000700563.2:c.1674+46C>A ENSP00000515066.2:n.1674+46C>A
ENST00000546498.2:n.361+46C>A
ENST00000700555.1:c.114+46C>A ENSP00000515062.1:n.114+46C>A
ENST00000700556.1:c.145+46C>A
ENST00000700559.1:c.889+46C>A
ENST00000700560.1:n.889+46C>A
ENST00000700561.1:n.1015+46C>A
ENST00000700563.1:c.1628+46C>A
ENST00000700564.1:n.1678+46C>A
ENST00000070846.11:c.1806+46C>A ENSP00000070846.6:n.1806+46C>A
ENST00000340811.9:c.1674+46C>A MANE Select ENSP00000342800.5:n.1674+46C>A
ENST00000070846.10:c.1806+46C>A ENSP00000070846.6:n.1806+46C>A
ENST00000340811.8:c.1674+46C>A ENSP00000342800.4:n.1674+46C>A
ENST00000546498.1:n.361+46C>A
ENST00000552612.5:n.95+46C>A
ENST00000613243.1:c.1806+46C>A ENSP00000478295.1:n.1806+46C>A
NM_001005242.2:c.1674+46C>A NP_001005242.2:n.1674+46C>A
NM_004572.3:c.1806+46C>A , LRG_398t1:c.1806+46C>A NP_004563.2:n.1806+46C>A
NM_001005242.3:c.1674+46C>A MANE Select NP_001005242.2:n.1674+46C>A
NM_004572.4:c.1806+46C>A NP_004563.2:n.1806+46C>A