Canonical Allele Identifier: CA384367236

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32993974G>C (hg19) ; chr12:g.32841040G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32841040G>C , CM000674.2:g.32841040G>C	GRCh38
NC_000012.11:g.32993974G>C , CM000674.1:g.32993974G>C	GRCh37
NC_000012.10:g.32885241G>C	NCBI36
NG_009000.1:g.60807C>G , LRG_398:g.60807C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000700559.2:c.1544C>G	ENSP00000515065.2:p.Thr515Ser
ENST00000700563.2:c.1544C>G	ENSP00000515066.2:p.Thr515Ser
ENST00000700556.1:c.15C>G
ENST00000700559.1:c.759C>G
ENST00000700560.1:n.759C>G
ENST00000700561.1:n.885C>G
ENST00000700563.1:c.1498C>G
ENST00000700564.1:n.1548C>G
ENST00000700565.1:n.1397C>G
ENST00000070846.11:c.1676C>G	ENSP00000070846.6:p.Thr559Ser
ENST00000340811.9:c.1544C>G MANE Select	ENSP00000342800.5:p.Thr515Ser
ENST00000070846.10:c.1676C>G	ENSP00000070846.6:p.Thr559Ser
ENST00000340811.8:c.1544C>G	ENSP00000342800.4:p.Thr515Ser
ENST00000613243.1:c.1676C>G	ENSP00000478295.1:p.Thr559Ser
NM_001005242.2:c.1544C>G	NP_001005242.2:p.Thr515Ser
NM_004572.3:c.1676C>G , LRG_398t1:c.1676C>G	NP_004563.2:p.Thr559Ser
NM_001005242.3:c.1544C>G MANE Select	NP_001005242.2:p.Thr515Ser
NM_004572.4:c.1676C>G	NP_004563.2:p.Thr559Ser