Canonical Allele Identifier: CA235265655

Gene: PKP2

Linked Data

• dbSNP Id: rs909838326
• gnomAD v4: 12-32877820-A-G
• MyVariant Identifiers: chr12:g.33030754A>G (hg19) ; chr12:g.32877820A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32877820A>G , CM000674.2:g.32877820A>G	GRCh38
NC_000012.11:g.33030754A>G , CM000674.1:g.33030754A>G	GRCh37
NC_000012.10:g.32922021A>G	NCBI36
NG_009000.1:g.24027T>C , LRG_398:g.24027T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700559.2:c.1034+26T>C	ENSP00000515065.2:n.1034+26T>C
ENST00000700563.2:c.1034+26T>C	ENSP00000515066.2:n.1034+26T>C
ENST00000700559.1:c.249+26T>C
ENST00000700560.1:n.249+26T>C
ENST00000700561.1:n.375+26T>C
ENST00000700563.1:c.988+26T>C
ENST00000700564.1:n.1038+26T>C
ENST00000700565.1:n.887+26T>C
ENST00000070846.11:c.1034+26T>C	ENSP00000070846.6:n.1034+26T>C
ENST00000340811.9:c.1034+26T>C MANE Select	ENSP00000342800.5:n.1034+26T>C
ENST00000070846.10:c.1034+26T>C	ENSP00000070846.6:n.1034+26T>C
ENST00000340811.8:c.1034+26T>C	ENSP00000342800.4:n.1034+26T>C
ENST00000613243.1:c.1034+26T>C	ENSP00000478295.1:n.1034+26T>C
NM_001005242.2:c.1034+26T>C	NP_001005242.2:n.1034+26T>C
NM_004572.3:c.1034+26T>C , LRG_398t1:c.1034+26T>C	NP_004563.2:n.1034+26T>C
NM_001005242.3:c.1034+26T>C MANE Select	NP_001005242.2:n.1034+26T>C
NM_004572.4:c.1034+26T>C	NP_004563.2:n.1034+26T>C