Canonical Allele Identifier: CA687449277

Gene: PKP2

Linked Data

• dbSNP Id: rs1444725014
• gnomAD v3: 12-32822738-TG-T
• gnomAD v4: 12-32822738-TG-T
• MyVariant Identifiers: chr12:g.32975673del (hg19) ; chr12:g.32822739del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822741del , CM000674.2:g.32822741del	GRCh38
NC_000012.11:g.32975675del , CM000674.1:g.32975675del	GRCh37
NC_000012.10:g.32866942del	NCBI36
NG_009000.1:g.79108del , LRG_398:g.79108del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.187-108del
ENST00000700559.2:c.1675-108del	ENSP00000515065.2:n.1675-108del
ENST00000700563.2:c.1675-108del	ENSP00000515066.2:n.1675-108del
ENST00000546498.2:n.362-108del
ENST00000700555.1:c.115-108del	ENSP00000515062.1:n.115-108del
ENST00000700556.1:c.146-108del
ENST00000700559.1:c.890-108del
ENST00000700560.1:n.890-108del
ENST00000700561.1:n.1016-108del
ENST00000700563.1:c.1629-108del
ENST00000700564.1:n.1679-108del
ENST00000070846.11:c.1807-108del	ENSP00000070846.6:n.1807-108del
ENST00000340811.9:c.1675-108del MANE Select	ENSP00000342800.5:n.1675-108del
ENST00000070846.10:c.1807-108del	ENSP00000070846.6:n.1807-108del
ENST00000340811.8:c.1675-108del	ENSP00000342800.4:n.1675-108del
ENST00000546498.1:n.362-108del
ENST00000552612.5:n.96-108del
ENST00000613243.1:c.1807-108del	ENSP00000478295.1:n.1807-108del
NM_001005242.2:c.1675-108del	NP_001005242.2:n.1675-108del
NM_004572.3:c.1807-108del , LRG_398t1:c.1807-108del	NP_004563.2:n.1807-108del
NM_001005242.3:c.1675-108del MANE Select	NP_001005242.2:n.1675-108del
NM_004572.4:c.1807-108del	NP_004563.2:n.1807-108del