Canonical Allele Identifier: CA2618226069

Gene: PKP2

Linked Data

• gnomAD v4: 12-32841332-GCCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32841333_32841335del , CM000674.2:g.32841333_32841335del	GRCh38
NC_000012.11:g.32994267_32994269del , CM000674.1:g.32994267_32994269del	GRCh37
NC_000012.10:g.32885534_32885536del	NCBI36
NG_009000.1:g.60512_60514del , LRG_398:g.60512_60514del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700559.2:c.1379-130_1379-128del	ENSP00000515065.2:n.1379-130_1379-128del
ENST00000700563.2:c.1379-130_1379-128del	ENSP00000515066.2:n.1379-130_1379-128del
ENST00000700559.1:c.594-130_594-128del
ENST00000700560.1:n.594-130_594-128del
ENST00000700561.1:n.720-130_720-128del
ENST00000700563.1:c.1333-130_1333-128del
ENST00000700564.1:n.1383-130_1383-128del
ENST00000700565.1:n.1232-130_1232-128del
ENST00000070846.11:c.1511-130_1511-128del	ENSP00000070846.6:n.1511-130_1511-128del
ENST00000340811.9:c.1379-130_1379-128del MANE Select	ENSP00000342800.5:n.1379-130_1379-128del
ENST00000070846.10:c.1511-130_1511-128del	ENSP00000070846.6:n.1511-130_1511-128del
ENST00000340811.8:c.1379-130_1379-128del	ENSP00000342800.4:n.1379-130_1379-128del
ENST00000613243.1:c.1511-130_1511-128del	ENSP00000478295.1:n.1511-130_1511-128del
NM_001005242.2:c.1379-130_1379-128del	NP_001005242.2:n.1379-130_1379-128del
NM_004572.3:c.1511-130_1511-128del , LRG_398t1:c.1511-130_1511-128del	NP_004563.2:n.1511-130_1511-128del
NM_001005242.3:c.1379-130_1379-128del MANE Select	NP_001005242.2:n.1379-130_1379-128del
NM_004572.4:c.1511-130_1511-128del	NP_004563.2:n.1511-130_1511-128del