Canonical Allele Identifier: CA422716469
Gene: PKP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.201286828C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201317700C>A , CM000663.2:g.201317700C>A GRCh38
NC_000001.10:g.201286828C>A , CM000663.1:g.201286828C>A GRCh37
NC_000001.9:g.199553451C>A NCBI36
NG_023337.1:g.39249C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367324.8:c.975C>A MANE Select ENSP00000356293.4:p.Thr325=
ENST00000263946.7:c.975C>A ENSP00000263946.3:p.Thr325=
ENST00000352845.3:c.975C>A ENSP00000295597.3:p.Thr325=
ENST00000367324.7:c.975C>A ENSP00000356293.3:p.Thr325=
ENST00000475988.1:n.317C>A
ENST00000622031.4:c.972C>A ENSP00000482213.1:p.Thr324=
NM_000299.3:c.975C>A NP_000290.2:p.Thr325=
NM_001005337.2:c.975C>A NP_001005337.1:p.Thr325=
NM_001005337.3:c.975C>A MANE Select NP_001005337.1:p.Thr325=
NM_000299.4:c.975C>A NP_000290.2:p.Thr325=