Canonical Allele Identifier: CA384366436

Gene: PKP2

Linked Data

• dbSNP Id: rs1956960849
• COSMIC: COSM3460270
• MyVariant Identifiers: chr12:g.33031882G>A (hg19) ; chr12:g.32878948G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32878948G>A , CM000674.2:g.32878948G>A	GRCh38
NC_000012.11:g.33031882G>A , CM000674.1:g.33031882G>A	GRCh37
NC_000012.10:g.32923149G>A	NCBI36
NG_009000.1:g.22899C>T , LRG_398:g.22899C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700559.2:c.308C>T	ENSP00000515065.2:p.Pro103Leu
ENST00000700563.2:c.308C>T	ENSP00000515066.2:p.Pro103Leu
ENST00000700563.1:c.262C>T
ENST00000700564.1:n.312C>T
ENST00000700565.1:n.161C>T
ENST00000070846.11:c.308C>T	ENSP00000070846.6:p.Pro103Leu
ENST00000340811.9:c.308C>T MANE Select	ENSP00000342800.5:p.Pro103Leu
ENST00000070846.10:c.308C>T	ENSP00000070846.6:p.Pro103Leu
ENST00000340811.8:c.308C>T	ENSP00000342800.4:p.Pro103Leu
ENST00000613243.1:c.308C>T	ENSP00000478295.1:p.Pro103Leu
NM_001005242.2:c.308C>T	NP_001005242.2:p.Pro103Leu
NM_004572.3:c.308C>T , LRG_398t1:c.308C>T	NP_004563.2:p.Pro103Leu
NM_001005242.3:c.308C>T MANE Select	NP_001005242.2:p.Pro103Leu
NM_004572.4:c.308C>T	NP_004563.2:p.Pro103Leu