Canonical Allele Identifier: CA384357569

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32949069T>A (hg19) ; chr12:g.32796135T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32796135T>A , CM000674.2:g.32796135T>A	GRCh38
NC_000012.11:g.32949069T>A , CM000674.1:g.32949069T>A	GRCh37
NC_000012.10:g.32840336T>A	NCBI36
NG_009000.1:g.105712A>T , LRG_398:g.105712A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.834A>T
ENST00000700557.2:n.423A>T
ENST00000700559.2:c.2168-3404A>T	ENSP00000515065.2:n.2168-3404A>T
ENST00000546498.2:n.1018A>T
ENST00000549461.2:n.823A>T
ENST00000700555.1:c.762A>T	ENSP00000515062.1:p.Lys254Asn
ENST00000700556.1:c.802A>T
ENST00000700557.1:c.342A>T	ENSP00000515064.1:p.Lys114Asn
ENST00000700558.1:n.545A>T
ENST00000700559.1:c.1383-3404A>T
ENST00000700560.1:n.1546A>T
ENST00000700561.1:n.1672A>T
ENST00000070846.11:c.2463A>T	ENSP00000070846.6:p.Lys821Asn
ENST00000340811.9:c.2331A>T MANE Select	ENSP00000342800.5:p.Lys777Asn
ENST00000070846.10:c.2463A>T	ENSP00000070846.6:p.Lys821Asn
ENST00000340811.8:c.2331A>T	ENSP00000342800.4:p.Lys777Asn
ENST00000613243.1:c.2461A>T	ENSP00000478295.1:p.Asn821Tyr
NM_001005242.2:c.2331A>T	NP_001005242.2:p.Lys777Asn
NM_004572.3:c.2463A>T , LRG_398t1:c.2463A>T	NP_004563.2:p.Lys821Asn
NM_001005242.3:c.2331A>T MANE Select	NP_001005242.2:p.Lys777Asn
NM_004572.4:c.2463A>T	NP_004563.2:p.Lys821Asn