Canonical Allele Identifier: CA16606521

Gene: PKP2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32841029T>A , CM000674.2:g.32841029T>A	GRCh38
NC_000012.11:g.32993963T>A , CM000674.1:g.32993963T>A	GRCh37
NC_000012.10:g.32885230T>A	NCBI36
NG_009000.1:g.60818A>T , LRG_398:g.60818A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700559.2:c.1555A>T	ENSP00000515065.2:p.Arg519Ter
ENST00000700563.2:c.1555A>T	ENSP00000515066.2:p.Arg519Ter
ENST00000700556.1:c.26A>T
ENST00000700559.1:c.770A>T
ENST00000700560.1:n.770A>T
ENST00000700561.1:n.896A>T
ENST00000700563.1:c.1509A>T
ENST00000700564.1:n.1559A>T
ENST00000700565.1:n.1408A>T
ENST00000070846.11:c.1687A>T	ENSP00000070846.6:p.Arg563Ter
ENST00000340811.9:c.1555A>T MANE Select	ENSP00000342800.5:p.Arg519Ter
ENST00000070846.10:c.1687A>T	ENSP00000070846.6:p.Arg563Ter
ENST00000340811.8:c.1555A>T	ENSP00000342800.4:p.Arg519Ter
ENST00000613243.1:c.1687A>T	ENSP00000478295.1:p.Arg563Ter
NM_001005242.2:c.1555A>T	NP_001005242.2:p.Arg519Ter
NM_004572.3:c.1687A>T , LRG_398t1:c.1687A>T	NP_004563.2:p.Arg563Ter
NM_001005242.3:c.1555A>T MANE Select	NP_001005242.2:p.Arg519Ter
NM_004572.4:c.1687A>T	NP_004563.2:p.Arg563Ter