Canonical Allele Identifier: CA235218660

Gene: PKP2

Linked Data

• dbSNP Id: rs866818266
• gnomAD v3: 12-32796634-C-T
• gnomAD v4: 12-32796634-C-T
• MyVariant Identifiers: chr12:g.32949568C>T (hg19) ; chr12:g.32796634C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32796634C>T , CM000674.2:g.32796634C>T	GRCh38
NC_000012.11:g.32949568C>T , CM000674.1:g.32949568C>T	GRCh37
NC_000012.10:g.32840835C>T	NCBI36
NG_009000.1:g.105213G>A , LRG_398:g.105213G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.671-336G>A
ENST00000700557.2:n.260-336G>A
ENST00000700559.2:c.2168-3903G>A	ENSP00000515065.2:n.2168-3903G>A
ENST00000546498.2:n.855-336G>A
ENST00000549461.2:n.660-336G>A
ENST00000700555.1:c.599-336G>A	ENSP00000515062.1:n.599-336G>A
ENST00000700556.1:c.639-336G>A
ENST00000700557.1:c.179-336G>A	ENSP00000515064.1:n.179-336G>A
ENST00000700558.1:n.382-336G>A
ENST00000700559.1:c.1383-3903G>A
ENST00000700560.1:n.1383-336G>A
ENST00000700561.1:n.1509-336G>A
ENST00000070846.11:c.2300-336G>A	ENSP00000070846.6:n.2300-336G>A
ENST00000340811.9:c.2168-336G>A MANE Select	ENSP00000342800.5:n.2168-336G>A
ENST00000070846.10:c.2300-336G>A	ENSP00000070846.6:n.2300-336G>A
ENST00000340811.8:c.2168-336G>A	ENSP00000342800.4:n.2168-336G>A
ENST00000613243.1:c.2300-336G>A	ENSP00000478295.1:n.2300-336G>A
NM_001005242.2:c.2168-336G>A	NP_001005242.2:n.2168-336G>A
NM_004572.3:c.2300-336G>A , LRG_398t1:c.2300-336G>A	NP_004563.2:n.2300-336G>A
NM_001005242.3:c.2168-336G>A MANE Select	NP_001005242.2:n.2168-336G>A
NM_004572.4:c.2300-336G>A	NP_004563.2:n.2300-336G>A