Canonical Allele Identifier: CA027088

Gene: PKP2

Linked Data

• ClinVar Variation Id: 565604
• ClinVar RCV Id: RCV000685202 ; RCV000773327 ; RCV001193943
• dbSNP Id: rs200586695
• ExAC: 12:33021917 C / T
• gnomAD v2: 12-33021917-C-T
• gnomAD v3: 12-32868983-C-T
• gnomAD v4: 12-32868983-C-T
• MyVariant Identifiers: chr12:g.33021917C>T (hg19) ; chr12:g.32868983C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32868983C>T , CM000674.2:g.32868983C>T	GRCh38
NC_000012.11:g.33021917C>T , CM000674.1:g.33021917C>T	GRCh37
NC_000012.10:g.32913184C>T	NCBI36
NG_009000.1:g.32864G>A , LRG_398:g.32864G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000700559.2:c.1114G>A	ENSP00000515065.2:p.Ala372Thr
ENST00000700563.2:c.1114G>A	ENSP00000515066.2:p.Ala372Thr
ENST00000700559.1:c.329G>A
ENST00000700560.1:n.329G>A
ENST00000700561.1:n.455G>A
ENST00000700563.1:c.1068G>A
ENST00000700564.1:n.1118G>A
ENST00000700565.1:n.967G>A
ENST00000070846.11:c.1114G>A	ENSP00000070846.6:p.Ala372Thr
ENST00000340811.9:c.1114G>A MANE Select	ENSP00000342800.5:p.Ala372Thr
ENST00000070846.10:c.1114G>A	ENSP00000070846.6:p.Ala372Thr
ENST00000340811.8:c.1114G>A	ENSP00000342800.4:p.Ala372Thr
ENST00000613243.1:c.1114G>A	ENSP00000478295.1:p.Ala372Thr
NM_001005242.2:c.1114G>A	NP_001005242.2:p.Ala372Thr
NM_004572.3:c.1114G>A , LRG_398t1:c.1114G>A	NP_004563.2:p.Ala372Thr
NM_001005242.3:c.1114G>A MANE Select	NP_001005242.2:p.Ala372Thr
NM_004572.4:c.1114G>A	NP_004563.2:p.Ala372Thr