Canonical Allele Identifier: CA384360075

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32955484T>C (hg19) ; chr12:g.32802550T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32802550T>C , CM000674.2:g.32802550T>C	GRCh38
NC_000012.11:g.32955484T>C , CM000674.1:g.32955484T>C	GRCh37
NC_000012.10:g.32846751T>C	NCBI36
NG_009000.1:g.99297A>G , LRG_398:g.99297A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.523A>G
ENST00000700557.2:n.112A>G
ENST00000700559.2:c.2020A>G	ENSP00000515065.2:p.Thr674Ala
ENST00000546498.2:n.707A>G
ENST00000549461.2:n.559A>G
ENST00000700555.1:c.451A>G	ENSP00000515062.1:p.Thr151Ala
ENST00000700556.1:c.491A>G
ENST00000700557.1:c.31A>G	ENSP00000515064.1:p.Thr11Ala
ENST00000700558.1:n.234A>G
ENST00000700559.1:c.1235A>G
ENST00000700560.1:n.1235A>G
ENST00000700561.1:n.1361A>G
ENST00000070846.11:c.2152A>G	ENSP00000070846.6:p.Thr718Ala
ENST00000340811.9:c.2020A>G MANE Select	ENSP00000342800.5:p.Thr674Ala
ENST00000070846.10:c.2152A>G	ENSP00000070846.6:p.Thr718Ala
ENST00000340811.8:c.2020A>G	ENSP00000342800.4:p.Thr674Ala
ENST00000549461.1:n.466A>G
ENST00000613243.1:c.2152A>G	ENSP00000478295.1:p.Thr718Ala
NM_001005242.2:c.2020A>G	NP_001005242.2:p.Thr674Ala
NM_004572.3:c.2152A>G , LRG_398t1:c.2152A>G	NP_004563.2:p.Thr718Ala
NM_001005242.3:c.2020A>G MANE Select	NP_001005242.2:p.Thr674Ala
NM_004572.4:c.2152A>G	NP_004563.2:p.Thr718Ala