Canonical Allele Identifier: CA422716439

Gene: PKP1

Linked Data

• MyVariant Identifiers: chr1:g.201286786G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201317658G>C , CM000663.2:g.201317658G>C	GRCh38
NC_000001.10:g.201286786G>C , CM000663.1:g.201286786G>C	GRCh37
NC_000001.9:g.199553409G>C	NCBI36
NG_023337.1:g.39207G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367324.8:c.933G>C MANE Select	ENSP00000356293.4:p.Leu311=
ENST00000263946.7:c.933G>C	ENSP00000263946.3:p.Leu311=
ENST00000352845.3:c.933G>C	ENSP00000295597.3:p.Leu311=
ENST00000367324.7:c.933G>C	ENSP00000356293.3:p.Leu311=
ENST00000475988.1:n.275G>C
ENST00000622031.4:c.930G>C	ENSP00000482213.1:p.Leu310=
NM_000299.3:c.933G>C	NP_000290.2:p.Leu311=
NM_001005337.2:c.933G>C	NP_001005337.1:p.Leu311=
NM_001005337.3:c.933G>C MANE Select	NP_001005337.1:p.Leu311=
NM_000299.4:c.933G>C	NP_000290.2:p.Leu311=