Canonical Allele Identifier: CA344178762
Gene: PKP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.201286895A>C (hg19) chr1:g.201317767A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201317767A>C , CM000663.2:g.201317767A>C GRCh38
NC_000001.10:g.201286895A>C , CM000663.1:g.201286895A>C GRCh37
NC_000001.9:g.199553518A>C NCBI36
NG_023337.1:g.39316A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367324.8:c.1042A>C MANE Select ENSP00000356293.4:p.Lys348Gln
ENST00000263946.7:c.1042A>C ENSP00000263946.3:p.Lys348Gln
ENST00000352845.3:c.1042A>C ENSP00000295597.3:p.Lys348Gln
ENST00000367324.7:c.1042A>C ENSP00000356293.3:p.Lys348Gln
ENST00000475988.1:n.384A>C
ENST00000622031.4:c.1039A>C ENSP00000482213.1:p.Lys347Gln
NM_000299.3:c.1042A>C NP_000290.2:p.Lys348Gln
NM_001005337.2:c.1042A>C NP_001005337.1:p.Lys348Gln
NM_001005337.3:c.1042A>C MANE Select NP_001005337.1:p.Lys348Gln
NM_000299.4:c.1042A>C NP_000290.2:p.Lys348Gln
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