Canonical Allele Identifier: CA604225835

Gene: PKP2

Linked Data

• dbSNP Id: rs1425584680
• gnomAD v2: 12-32975654-AG-A
• gnomAD v3: 12-32822720-AG-A
• gnomAD v4: 12-32822720-AG-A
• MyVariant Identifiers: chr12:g.32975655del (hg19) ; chr12:g.32822721del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822722del , CM000674.2:g.32822722del	GRCh38
NC_000012.11:g.32975656del , CM000674.1:g.32975656del	GRCh37
NC_000012.10:g.32866923del	NCBI36
NG_009000.1:g.79126del , LRG_398:g.79126del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.187-90del
ENST00000700559.2:c.1675-90del	ENSP00000515065.2:n.1675-90del
ENST00000700563.2:c.1675-90del	ENSP00000515066.2:n.1675-90del
ENST00000546498.2:n.362-90del
ENST00000700555.1:c.115-90del	ENSP00000515062.1:n.115-90del
ENST00000700556.1:c.146-90del
ENST00000700559.1:c.890-90del
ENST00000700560.1:n.890-90del
ENST00000700561.1:n.1016-90del
ENST00000700563.1:c.1629-90del
ENST00000700564.1:n.1679-90del
ENST00000070846.11:c.1807-90del	ENSP00000070846.6:n.1807-90del
ENST00000340811.9:c.1675-90del MANE Select	ENSP00000342800.5:n.1675-90del
ENST00000070846.10:c.1807-90del	ENSP00000070846.6:n.1807-90del
ENST00000340811.8:c.1675-90del	ENSP00000342800.4:n.1675-90del
ENST00000546498.1:n.362-90del
ENST00000552612.5:n.96-90del
ENST00000613243.1:c.1807-90del	ENSP00000478295.1:n.1807-90del
NM_001005242.2:c.1675-90del	NP_001005242.2:n.1675-90del
NM_004572.3:c.1807-90del , LRG_398t1:c.1807-90del	NP_004563.2:n.1807-90del
NM_001005242.3:c.1675-90del MANE Select	NP_001005242.2:n.1675-90del
NM_004572.4:c.1807-90del	NP_004563.2:n.1807-90del