Canonical Allele Identifier: CA384367982
Gene: PKP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32841160A>C , CM000674.2:g.32841160A>C GRCh38
NC_000012.11:g.32994094A>C , CM000674.1:g.32994094A>C GRCh37
NC_000012.10:g.32885361A>C NCBI36
NG_009000.1:g.60687T>G , LRG_398:g.60687T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700559.2:c.1424T>G ENSP00000515065.2:p.Met475Arg
ENST00000700563.2:c.1424T>G ENSP00000515066.2:p.Met475Arg
ENST00000700559.1:c.639T>G
ENST00000700560.1:n.639T>G
ENST00000700561.1:n.765T>G
ENST00000700563.1:c.1378T>G
ENST00000700564.1:n.1428T>G
ENST00000700565.1:n.1277T>G
ENST00000070846.11:c.1556T>G ENSP00000070846.6:p.Met519Arg
ENST00000340811.9:c.1424T>G MANE Select ENSP00000342800.5:p.Met475Arg
ENST00000070846.10:c.1556T>G ENSP00000070846.6:p.Met519Arg
ENST00000340811.8:c.1424T>G ENSP00000342800.4:p.Met475Arg
ENST00000613243.1:c.1556T>G ENSP00000478295.1:p.Met519Arg
NM_001005242.2:c.1424T>G NP_001005242.2:p.Met475Arg
NM_004572.3:c.1556T>G , LRG_398t1:c.1556T>G NP_004563.2:p.Met519Arg
NM_001005242.3:c.1424T>G MANE Select NP_001005242.2:p.Met475Arg
NM_004572.4:c.1556T>G NP_004563.2:p.Met519Arg