Canonical Allele Identifier: CA422716490
Gene: PKP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.201286843G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201317715G>C , CM000663.2:g.201317715G>C GRCh38
NC_000001.10:g.201286843G>C , CM000663.1:g.201286843G>C GRCh37
NC_000001.9:g.199553466G>C NCBI36
NG_023337.1:g.39264G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367324.8:c.990G>C MANE Select ENSP00000356293.4:p.Gly330=
ENST00000263946.7:c.990G>C ENSP00000263946.3:p.Gly330=
ENST00000352845.3:c.990G>C ENSP00000295597.3:p.Gly330=
ENST00000367324.7:c.990G>C ENSP00000356293.3:p.Gly330=
ENST00000475988.1:n.332G>C
ENST00000622031.4:c.987G>C ENSP00000482213.1:p.Gly329=
NM_000299.3:c.990G>C NP_000290.2:p.Gly330=
NM_001005337.2:c.990G>C NP_001005337.1:p.Gly330=
NM_001005337.3:c.990G>C MANE Select NP_001005337.1:p.Gly330=
NM_000299.4:c.990G>C NP_000290.2:p.Gly330=