Canonical Allele Identifier: CA344178118
Gene: PKP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.201286740T>A (hg19) chr1:g.201317612T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201317612T>A , CM000663.2:g.201317612T>A GRCh38
NC_000001.10:g.201286740T>A , CM000663.1:g.201286740T>A GRCh37
NC_000001.9:g.199553363T>A NCBI36
NG_023337.1:g.39161T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367324.8:c.887T>A MANE Select ENSP00000356293.4:p.Leu296His
ENST00000263946.7:c.887T>A ENSP00000263946.3:p.Leu296His
ENST00000352845.3:c.887T>A ENSP00000295597.3:p.Leu296His
ENST00000367324.7:c.887T>A ENSP00000356293.3:p.Leu296His
ENST00000475988.1:n.229T>A
ENST00000622031.4:c.884T>A ENSP00000482213.1:p.Leu295His
NM_000299.3:c.887T>A NP_000290.2:p.Leu296His
NM_001005337.2:c.887T>A NP_001005337.1:p.Leu296His
NM_001005337.3:c.887T>A MANE Select NP_001005337.1:p.Leu296His
NM_000299.4:c.887T>A NP_000290.2:p.Leu296His
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