Canonical Allele Identifier: CA036591
Community Standard Title: NM_001005242.3(PKP2):c.313C>G (p.Pro105Ala)
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32878943G>C , CM000674.2:g.32878943G>C GRCh38
NC_000012.11:g.33031877G>C , CM000674.1:g.33031877G>C GRCh37
NC_000012.10:g.32923144G>C NCBI36
NG_009000.1:g.22904C>G , LRG_398:g.22904C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001005242.3:c.313C>G MANE Select NP_001005242.2:p.Pro105Ala
ENST00000340811.9:c.313C>G MANE Select ENSP00000342800.5:p.Pro105Ala
NM_001005242.2:c.313C>G NP_001005242.2:p.Pro105Ala
NM_004572.3:c.313C>G , LRG_398t1:c.313C>G NP_004563.2:p.Pro105Ala
NM_004572.4:c.313C>G NP_004563.2:p.Pro105Ala
ENST00000070846.10:c.313C>G ENSP00000070846.6:p.Pro105Ala
ENST00000070846.11:c.313C>G ENSP00000070846.6:p.Pro105Ala
ENST00000340811.8:c.313C>G ENSP00000342800.4:p.Pro105Ala
ENST00000613243.1:c.313C>G ENSP00000478295.1:p.Pro105Ala
ENST00000700559.2:c.313C>G ENSP00000515065.2:p.Pro105Ala
ENST00000700563.1:c.267C>G
ENST00000700563.2:c.313C>G ENSP00000515066.2:p.Pro105Ala
ENST00000700564.1:n.317C>G
ENST00000700565.1:n.166C>G