Canonical Allele Identifier: CA479174994
Gene: PKP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.33031908T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32878974T>C , CM000674.2:g.32878974T>C GRCh38
NC_000012.11:g.33031908T>C , CM000674.1:g.33031908T>C GRCh37
NC_000012.10:g.32923175T>C NCBI36
NG_009000.1:g.22873A>G , LRG_398:g.22873A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700559.2:c.282A>G ENSP00000515065.2:p.Glu94=
ENST00000700563.2:c.282A>G ENSP00000515066.2:p.Glu94=
ENST00000700563.1:c.236A>G
ENST00000700564.1:n.286A>G
ENST00000700565.1:n.135A>G
ENST00000070846.11:c.282A>G ENSP00000070846.6:p.Glu94=
ENST00000340811.9:c.282A>G MANE Select ENSP00000342800.5:p.Glu94=
ENST00000070846.10:c.282A>G ENSP00000070846.6:p.Glu94=
ENST00000340811.8:c.282A>G ENSP00000342800.4:p.Glu94=
ENST00000613243.1:c.282A>G ENSP00000478295.1:p.Glu94=
NM_001005242.2:c.282A>G NP_001005242.2:p.Glu94=
NM_004572.3:c.282A>G , LRG_398t1:c.282A>G NP_004563.2:p.Glu94=
NM_001005242.3:c.282A>G MANE Select NP_001005242.2:p.Glu94=
NM_004572.4:c.282A>G NP_004563.2:p.Glu94=