Canonical Allele Identifier: CA479177242

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32993988T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32841054T>G , CM000674.2:g.32841054T>G	GRCh38
NC_000012.11:g.32993988T>G , CM000674.1:g.32993988T>G	GRCh37
NC_000012.10:g.32885255T>G	NCBI36
NG_009000.1:g.60793A>C , LRG_398:g.60793A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000700559.2:c.1530A>C	ENSP00000515065.2:p.Ile510=
ENST00000700563.2:c.1530A>C	ENSP00000515066.2:p.Ile510=
ENST00000700556.1:c.1A>C
ENST00000700559.1:c.745A>C
ENST00000700560.1:n.745A>C
ENST00000700561.1:n.871A>C
ENST00000700563.1:c.1484A>C
ENST00000700564.1:n.1534A>C
ENST00000700565.1:n.1383A>C
ENST00000070846.11:c.1662A>C	ENSP00000070846.6:p.Ile554=
ENST00000340811.9:c.1530A>C MANE Select	ENSP00000342800.5:p.Ile510=
ENST00000070846.10:c.1662A>C	ENSP00000070846.6:p.Ile554=
ENST00000340811.8:c.1530A>C	ENSP00000342800.4:p.Ile510=
ENST00000613243.1:c.1662A>C	ENSP00000478295.1:p.Ile554=
NM_001005242.2:c.1530A>C	NP_001005242.2:p.Ile510=
NM_004572.3:c.1662A>C , LRG_398t1:c.1662A>C	NP_004563.2:p.Ile554=
NM_001005242.3:c.1530A>C MANE Select	NP_001005242.2:p.Ile510=
NM_004572.4:c.1662A>C	NP_004563.2:p.Ile554=