Canonical Allele Identifier: CA2618226456

Gene: PKP2

Linked Data

• gnomAD v4: 12-32868901-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32868901T>C , CM000674.2:g.32868901T>C	GRCh38
NC_000012.11:g.33021835T>C , CM000674.1:g.33021835T>C	GRCh37
NC_000012.10:g.32913102T>C	NCBI36
NG_009000.1:g.32946A>G , LRG_398:g.32946A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000700559.2:c.1170+26A>G	ENSP00000515065.2:n.1170+26A>G
ENST00000700563.2:c.1170+26A>G	ENSP00000515066.2:n.1170+26A>G
ENST00000700559.1:c.385+26A>G
ENST00000700560.1:n.385+26A>G
ENST00000700561.1:n.511+26A>G
ENST00000700563.1:c.1124+26A>G
ENST00000700564.1:n.1174+26A>G
ENST00000700565.1:n.1023+26A>G
ENST00000070846.11:c.1170+26A>G	ENSP00000070846.6:n.1170+26A>G
ENST00000340811.9:c.1170+26A>G MANE Select	ENSP00000342800.5:n.1170+26A>G
ENST00000070846.10:c.1170+26A>G	ENSP00000070846.6:n.1170+26A>G
ENST00000340811.8:c.1170+26A>G	ENSP00000342800.4:n.1170+26A>G
ENST00000613243.1:c.1170+26A>G	ENSP00000478295.1:n.1170+26A>G
NM_001005242.2:c.1170+26A>G	NP_001005242.2:n.1170+26A>G
NM_004572.3:c.1170+26A>G , LRG_398t1:c.1170+26A>G	NP_004563.2:n.1170+26A>G
NM_001005242.3:c.1170+26A>G MANE Select	NP_001005242.2:n.1170+26A>G
NM_004572.4:c.1170+26A>G	NP_004563.2:n.1170+26A>G