Canonical Allele Identifier: CA384357930

Gene: PKP2

Linked Data

• COSMIC: COSM6072448
• MyVariant Identifiers: chr12:g.32949210C>G (hg19) ; chr12:g.32796276C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32796276C>G , CM000674.2:g.32796276C>G	GRCh38
NC_000012.11:g.32949210C>G , CM000674.1:g.32949210C>G	GRCh37
NC_000012.10:g.32840477C>G	NCBI36
NG_009000.1:g.105571G>C , LRG_398:g.105571G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.693G>C
ENST00000700557.2:n.282G>C
ENST00000700559.2:c.2168-3545G>C	ENSP00000515065.2:n.2168-3545G>C
ENST00000546498.2:n.877G>C
ENST00000549461.2:n.682G>C
ENST00000700555.1:c.621G>C	ENSP00000515062.1:p.Leu207Phe
ENST00000700556.1:c.661G>C
ENST00000700557.1:c.201G>C	ENSP00000515064.1:p.Leu67Phe
ENST00000700558.1:n.404G>C
ENST00000700559.1:c.1383-3545G>C
ENST00000700560.1:n.1405G>C
ENST00000700561.1:n.1531G>C
ENST00000070846.11:c.2322G>C	ENSP00000070846.6:p.Leu774Phe
ENST00000340811.9:c.2190G>C MANE Select	ENSP00000342800.5:p.Leu730Phe
ENST00000070846.10:c.2322G>C	ENSP00000070846.6:p.Leu774Phe
ENST00000340811.8:c.2190G>C	ENSP00000342800.4:p.Leu730Phe
ENST00000613243.1:c.2322G>C	ENSP00000478295.1:p.Leu774Phe
NM_001005242.2:c.2190G>C	NP_001005242.2:p.Leu730Phe
NM_004572.3:c.2322G>C , LRG_398t1:c.2322G>C	NP_004563.2:p.Leu774Phe
NM_001005242.3:c.2190G>C MANE Select	NP_001005242.2:p.Leu730Phe
NM_004572.4:c.2322G>C	NP_004563.2:p.Leu774Phe