Canonical Allele Identifier: CA479177297

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32994081T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32841147T>G , CM000674.2:g.32841147T>G	GRCh38
NC_000012.11:g.32994081T>G , CM000674.1:g.32994081T>G	GRCh37
NC_000012.10:g.32885348T>G	NCBI36
NG_009000.1:g.60700A>C , LRG_398:g.60700A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700559.2:c.1437A>C	ENSP00000515065.2:p.Ala479=
ENST00000700563.2:c.1437A>C	ENSP00000515066.2:p.Ala479=
ENST00000700559.1:c.652A>C
ENST00000700560.1:n.652A>C
ENST00000700561.1:n.778A>C
ENST00000700563.1:c.1391A>C
ENST00000700564.1:n.1441A>C
ENST00000700565.1:n.1290A>C
ENST00000070846.11:c.1569A>C	ENSP00000070846.6:p.Ala523=
ENST00000340811.9:c.1437A>C MANE Select	ENSP00000342800.5:p.Ala479=
ENST00000070846.10:c.1569A>C	ENSP00000070846.6:p.Ala523=
ENST00000340811.8:c.1437A>C	ENSP00000342800.4:p.Ala479=
ENST00000613243.1:c.1569A>C	ENSP00000478295.1:p.Ala523=
NM_001005242.2:c.1437A>C	NP_001005242.2:p.Ala479=
NM_004572.3:c.1569A>C , LRG_398t1:c.1569A>C	NP_004563.2:p.Ala523=
NM_001005242.3:c.1437A>C MANE Select	NP_001005242.2:p.Ala479=
NM_004572.4:c.1569A>C	NP_004563.2:p.Ala523=