Canonical Allele Identifier: CA384363156

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32975486T>G (hg19) ; chr12:g.32822552T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822552T>G , CM000674.2:g.32822552T>G	GRCh38
NC_000012.11:g.32975486T>G , CM000674.1:g.32975486T>G	GRCh37
NC_000012.10:g.32866753T>G	NCBI36
NG_009000.1:g.79295A>C , LRG_398:g.79295A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000700555.2:n.266A>C
ENST00000700559.2:c.1754A>C	ENSP00000515065.2:p.Asn585Thr
ENST00000700563.2:c.1754A>C	ENSP00000515066.2:p.Asn585Thr
ENST00000546498.2:n.441A>C
ENST00000700555.1:c.194A>C	ENSP00000515062.1:p.Asn65Thr
ENST00000700556.1:c.225A>C
ENST00000700559.1:c.969A>C
ENST00000700560.1:n.969A>C
ENST00000700561.1:n.1095A>C
ENST00000700563.1:c.1708A>C
ENST00000700564.1:n.1758A>C
ENST00000070846.11:c.1886A>C	ENSP00000070846.6:p.Asn629Thr
ENST00000340811.9:c.1754A>C MANE Select	ENSP00000342800.5:p.Asn585Thr
ENST00000070846.10:c.1886A>C	ENSP00000070846.6:p.Asn629Thr
ENST00000340811.8:c.1754A>C	ENSP00000342800.4:p.Asn585Thr
ENST00000546498.1:n.441A>C
ENST00000552612.5:n.175A>C
ENST00000613243.1:c.1886A>C	ENSP00000478295.1:p.Asn629Thr
NM_001005242.2:c.1754A>C	NP_001005242.2:p.Asn585Thr
NM_004572.3:c.1886A>C , LRG_398t1:c.1886A>C	NP_004563.2:p.Asn629Thr
NM_001005242.3:c.1754A>C MANE Select	NP_001005242.2:p.Asn585Thr
NM_004572.4:c.1886A>C	NP_004563.2:p.Asn629Thr