Canonical Allele Identifier: CA384363547

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32975543A>T (hg19) ; chr12:g.32822609A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822609A>T , CM000674.2:g.32822609A>T	GRCh38
NC_000012.11:g.32975543A>T , CM000674.1:g.32975543A>T	GRCh37
NC_000012.10:g.32866810A>T	NCBI36
NG_009000.1:g.79238T>A , LRG_398:g.79238T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.209T>A
ENST00000700559.2:c.1697T>A	ENSP00000515065.2:p.Ile566Asn
ENST00000700563.2:c.1697T>A	ENSP00000515066.2:p.Ile566Asn
ENST00000546498.2:n.384T>A
ENST00000700555.1:c.137T>A	ENSP00000515062.1:p.Ile46Asn
ENST00000700556.1:c.168T>A
ENST00000700559.1:c.912T>A
ENST00000700560.1:n.912T>A
ENST00000700561.1:n.1038T>A
ENST00000700563.1:c.1651T>A
ENST00000700564.1:n.1701T>A
ENST00000070846.11:c.1829T>A	ENSP00000070846.6:p.Ile610Asn
ENST00000340811.9:c.1697T>A MANE Select	ENSP00000342800.5:p.Ile566Asn
ENST00000070846.10:c.1829T>A	ENSP00000070846.6:p.Ile610Asn
ENST00000340811.8:c.1697T>A	ENSP00000342800.4:p.Ile566Asn
ENST00000546498.1:n.384T>A
ENST00000552612.5:n.118T>A
ENST00000613243.1:c.1829T>A	ENSP00000478295.1:p.Ile610Asn
NM_001005242.2:c.1697T>A	NP_001005242.2:p.Ile566Asn
NM_004572.3:c.1829T>A , LRG_398t1:c.1829T>A	NP_004563.2:p.Ile610Asn
NM_001005242.3:c.1697T>A MANE Select	NP_001005242.2:p.Ile566Asn
NM_004572.4:c.1829T>A	NP_004563.2:p.Ile610Asn