Canonical Allele Identifier: CA479176232

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32975410T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822476T>C , CM000674.2:g.32822476T>C	GRCh38
NC_000012.11:g.32975410T>C , CM000674.1:g.32975410T>C	GRCh37
NC_000012.10:g.32866677T>C	NCBI36
NG_009000.1:g.79371A>G , LRG_398:g.79371A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.342A>G
ENST00000700559.2:c.1830A>G	ENSP00000515065.2:p.Lys610=
ENST00000700563.2:c.1830A>G	ENSP00000515066.2:p.Lys610=
ENST00000546498.2:n.517A>G
ENST00000700555.1:c.270A>G	ENSP00000515062.1:p.Lys90=
ENST00000700556.1:c.301A>G
ENST00000700559.1:c.1045A>G
ENST00000700560.1:n.1045A>G
ENST00000700561.1:n.1171A>G
ENST00000700563.1:c.1784A>G
ENST00000700564.1:n.1834A>G
ENST00000070846.11:c.1962A>G	ENSP00000070846.6:p.Lys654=
ENST00000340811.9:c.1830A>G MANE Select	ENSP00000342800.5:p.Lys610=
ENST00000070846.10:c.1962A>G	ENSP00000070846.6:p.Lys654=
ENST00000340811.8:c.1830A>G	ENSP00000342800.4:p.Lys610=
ENST00000546498.1:n.517A>G
ENST00000552612.5:n.251A>G
ENST00000613243.1:c.1962A>G	ENSP00000478295.1:p.Lys654=
NM_001005242.2:c.1830A>G	NP_001005242.2:p.Lys610=
NM_004572.3:c.1962A>G , LRG_398t1:c.1962A>G	NP_004563.2:p.Lys654=
NM_001005242.3:c.1830A>G MANE Select	NP_001005242.2:p.Lys610=
NM_004572.4:c.1962A>G	NP_004563.2:p.Lys654=