Canonical Allele Identifier: CA422716406
Gene: PKP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.201286735C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201317607C>T , CM000663.2:g.201317607C>T GRCh38
NC_000001.10:g.201286735C>T , CM000663.1:g.201286735C>T GRCh37
NC_000001.9:g.199553358C>T NCBI36
NG_023337.1:g.39156C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367324.8:c.882C>T MANE Select ENSP00000356293.4:p.Asp294=
ENST00000263946.7:c.882C>T ENSP00000263946.3:p.Asp294=
ENST00000352845.3:c.882C>T ENSP00000295597.3:p.Asp294=
ENST00000367324.7:c.882C>T ENSP00000356293.3:p.Asp294=
ENST00000475988.1:n.224C>T
ENST00000622031.4:c.879C>T ENSP00000482213.1:p.Asp293=
NM_000299.3:c.882C>T NP_000290.2:p.Asp294=
NM_001005337.2:c.882C>T NP_001005337.1:p.Asp294=
NM_001005337.3:c.882C>T MANE Select NP_001005337.1:p.Asp294=
NM_000299.4:c.882C>T NP_000290.2:p.Asp294=