Canonical Allele Identifier: CA422716475
Gene: PKP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.201286831G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201317703G>A , CM000663.2:g.201317703G>A GRCh38
NC_000001.10:g.201286831G>A , CM000663.1:g.201286831G>A GRCh37
NC_000001.9:g.199553454G>A NCBI36
NG_023337.1:g.39252G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367324.8:c.978G>A MANE Select ENSP00000356293.4:p.Arg326=
ENST00000263946.7:c.978G>A ENSP00000263946.3:p.Arg326=
ENST00000352845.3:c.978G>A ENSP00000295597.3:p.Arg326=
ENST00000367324.7:c.978G>A ENSP00000356293.3:p.Arg326=
ENST00000475988.1:n.320G>A
ENST00000622031.4:c.975G>A ENSP00000482213.1:p.Arg325=
NM_000299.3:c.978G>A NP_000290.2:p.Arg326=
NM_001005337.2:c.978G>A NP_001005337.1:p.Arg326=
NM_001005337.3:c.978G>A MANE Select NP_001005337.1:p.Arg326=
NM_000299.4:c.978G>A NP_000290.2:p.Arg326=