Canonical Allele Identifier: CA730093484

Gene: PKP1

Linked Data

• dbSNP Id: rs1170655675
• gnomAD v3: 1-201318069-C-T
• gnomAD v4: 1-201318069-C-T
• MyVariant Identifiers: chr1:g.201287197C>T (hg19) ; chr1:g.201318069C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201318069C>T , CM000663.2:g.201318069C>T	GRCh38
NC_000001.10:g.201287197C>T , CM000663.1:g.201287197C>T	GRCh37
NC_000001.9:g.199553820C>T	NCBI36
NG_023337.1:g.39618C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367324.8:c.1054+290C>T MANE Select	ENSP00000356293.4:n.1054+290C>T
ENST00000263946.7:c.1054+290C>T	ENSP00000263946.3:n.1054+290C>T
ENST00000352845.3:c.1054+290C>T	ENSP00000295597.3:n.1054+290C>T
ENST00000367324.7:c.1054+290C>T	ENSP00000356293.3:n.1054+290C>T
ENST00000475988.1:n.396+290C>T
ENST00000622031.4:c.1051+290C>T	ENSP00000482213.1:n.1051+290C>T
NM_000299.3:c.1054+290C>T	NP_000290.2:n.1054+290C>T
NM_001005337.2:c.1054+290C>T	NP_001005337.1:n.1054+290C>T
NM_001005337.3:c.1054+290C>T MANE Select	NP_001005337.1:n.1054+290C>T
NM_000299.4:c.1054+290C>T	NP_000290.2:n.1054+290C>T