Canonical Allele Identifier: CA384363466

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32975534T>G (hg19) ; chr12:g.32822600T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822600T>G , CM000674.2:g.32822600T>G	GRCh38
NC_000012.11:g.32975534T>G , CM000674.1:g.32975534T>G	GRCh37
NC_000012.10:g.32866801T>G	NCBI36
NG_009000.1:g.79247A>C , LRG_398:g.79247A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.218A>C
ENST00000700559.2:c.1706A>C	ENSP00000515065.2:p.Asn569Thr
ENST00000700563.2:c.1706A>C	ENSP00000515066.2:p.Asn569Thr
ENST00000546498.2:n.393A>C
ENST00000700555.1:c.146A>C	ENSP00000515062.1:p.Asn49Thr
ENST00000700556.1:c.177A>C
ENST00000700559.1:c.921A>C
ENST00000700560.1:n.921A>C
ENST00000700561.1:n.1047A>C
ENST00000700563.1:c.1660A>C
ENST00000700564.1:n.1710A>C
ENST00000070846.11:c.1838A>C	ENSP00000070846.6:p.Asn613Thr
ENST00000340811.9:c.1706A>C MANE Select	ENSP00000342800.5:p.Asn569Thr
ENST00000070846.10:c.1838A>C	ENSP00000070846.6:p.Asn613Thr
ENST00000340811.8:c.1706A>C	ENSP00000342800.4:p.Asn569Thr
ENST00000546498.1:n.393A>C
ENST00000552612.5:n.127A>C
ENST00000613243.1:c.1838A>C	ENSP00000478295.1:p.Asn613Thr
NM_001005242.2:c.1706A>C	NP_001005242.2:p.Asn569Thr
NM_004572.3:c.1838A>C , LRG_398t1:c.1838A>C	NP_004563.2:p.Asn613Thr
NM_001005242.3:c.1706A>C MANE Select	NP_001005242.2:p.Asn569Thr
NM_004572.4:c.1838A>C	NP_004563.2:p.Asn613Thr