Canonical Allele Identifier: CA422716491
Gene: PKP1 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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