Canonical Allele Identifier: CA384362816

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32975446G>C (hg19) ; chr12:g.32822512G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822512G>C , CM000674.2:g.32822512G>C	GRCh38
NC_000012.11:g.32975446G>C , CM000674.1:g.32975446G>C	GRCh37
NC_000012.10:g.32866713G>C	NCBI36
NG_009000.1:g.79335C>G , LRG_398:g.79335C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.306C>G
ENST00000700559.2:c.1794C>G	ENSP00000515065.2:p.Asn598Lys
ENST00000700563.2:c.1794C>G	ENSP00000515066.2:p.Asn598Lys
ENST00000546498.2:n.481C>G
ENST00000700555.1:c.234C>G	ENSP00000515062.1:p.Asn78Lys
ENST00000700556.1:c.265C>G
ENST00000700559.1:c.1009C>G
ENST00000700560.1:n.1009C>G
ENST00000700561.1:n.1135C>G
ENST00000700563.1:c.1748C>G
ENST00000700564.1:n.1798C>G
ENST00000070846.11:c.1926C>G	ENSP00000070846.6:p.Asn642Lys
ENST00000340811.9:c.1794C>G MANE Select	ENSP00000342800.5:p.Asn598Lys
ENST00000070846.10:c.1926C>G	ENSP00000070846.6:p.Asn642Lys
ENST00000340811.8:c.1794C>G	ENSP00000342800.4:p.Asn598Lys
ENST00000546498.1:n.481C>G
ENST00000552612.5:n.215C>G
ENST00000613243.1:c.1926C>G	ENSP00000478295.1:p.Asn642Lys
NM_001005242.2:c.1794C>G	NP_001005242.2:p.Asn598Lys
NM_004572.3:c.1926C>G , LRG_398t1:c.1926C>G	NP_004563.2:p.Asn642Lys
NM_001005242.3:c.1794C>G MANE Select	NP_001005242.2:p.Asn598Lys
NM_004572.4:c.1926C>G	NP_004563.2:p.Asn642Lys