Canonical Allele Identifier: CA479174547

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.33021870A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32868936A>C , CM000674.2:g.32868936A>C	GRCh38
NC_000012.11:g.33021870A>C , CM000674.1:g.33021870A>C	GRCh37
NC_000012.10:g.32913137A>C	NCBI36
NG_009000.1:g.32911T>G , LRG_398:g.32911T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700559.2:c.1161T>G	ENSP00000515065.2:p.Ala387=
ENST00000700563.2:c.1161T>G	ENSP00000515066.2:p.Ala387=
ENST00000700559.1:c.376T>G
ENST00000700560.1:n.376T>G
ENST00000700561.1:n.502T>G
ENST00000700563.1:c.1115T>G
ENST00000700564.1:n.1165T>G
ENST00000700565.1:n.1014T>G
ENST00000070846.11:c.1161T>G	ENSP00000070846.6:p.Ala387=
ENST00000340811.9:c.1161T>G MANE Select	ENSP00000342800.5:p.Ala387=
ENST00000070846.10:c.1161T>G	ENSP00000070846.6:p.Ala387=
ENST00000340811.8:c.1161T>G	ENSP00000342800.4:p.Ala387=
ENST00000613243.1:c.1161T>G	ENSP00000478295.1:p.Ala387=
NM_001005242.2:c.1161T>G	NP_001005242.2:p.Ala387=
NM_004572.3:c.1161T>G , LRG_398t1:c.1161T>G	NP_004563.2:p.Ala387=
NM_001005242.3:c.1161T>G MANE Select	NP_001005242.2:p.Ala387=
NM_004572.4:c.1161T>G	NP_004563.2:p.Ala387=