Canonical Allele Identifier: CA422716422
Gene: PKP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.201286762C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201317634C>G , CM000663.2:g.201317634C>G GRCh38
NC_000001.10:g.201286762C>G , CM000663.1:g.201286762C>G GRCh37
NC_000001.9:g.199553385C>G NCBI36
NG_023337.1:g.39183C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367324.8:c.909C>G MANE Select ENSP00000356293.4:p.Val303=
ENST00000263946.7:c.909C>G ENSP00000263946.3:p.Val303=
ENST00000352845.3:c.909C>G ENSP00000295597.3:p.Val303=
ENST00000367324.7:c.909C>G ENSP00000356293.3:p.Val303=
ENST00000475988.1:n.251C>G
ENST00000622031.4:c.906C>G ENSP00000482213.1:p.Val302=
NM_000299.3:c.909C>G NP_000290.2:p.Val303=
NM_001005337.2:c.909C>G NP_001005337.1:p.Val303=
NM_001005337.3:c.909C>G MANE Select NP_001005337.1:p.Val303=
NM_000299.4:c.909C>G NP_000290.2:p.Val303=