Canonical Allele Identifier: CA479176250

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32975443T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822509T>C , CM000674.2:g.32822509T>C	GRCh38
NC_000012.11:g.32975443T>C , CM000674.1:g.32975443T>C	GRCh37
NC_000012.10:g.32866710T>C	NCBI36
NG_009000.1:g.79338A>G , LRG_398:g.79338A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.309A>G
ENST00000700559.2:c.1797A>G	ENSP00000515065.2:p.Lys599=
ENST00000700563.2:c.1797A>G	ENSP00000515066.2:p.Lys599=
ENST00000546498.2:n.484A>G
ENST00000700555.1:c.237A>G	ENSP00000515062.1:p.Lys79=
ENST00000700556.1:c.268A>G
ENST00000700559.1:c.1012A>G
ENST00000700560.1:n.1012A>G
ENST00000700561.1:n.1138A>G
ENST00000700563.1:c.1751A>G
ENST00000700564.1:n.1801A>G
ENST00000070846.11:c.1929A>G	ENSP00000070846.6:p.Lys643=
ENST00000340811.9:c.1797A>G MANE Select	ENSP00000342800.5:p.Lys599=
ENST00000070846.10:c.1929A>G	ENSP00000070846.6:p.Lys643=
ENST00000340811.8:c.1797A>G	ENSP00000342800.4:p.Lys599=
ENST00000546498.1:n.484A>G
ENST00000552612.5:n.218A>G
ENST00000613243.1:c.1929A>G	ENSP00000478295.1:p.Lys643=
NM_001005242.2:c.1797A>G	NP_001005242.2:p.Lys599=
NM_004572.3:c.1929A>G , LRG_398t1:c.1929A>G	NP_004563.2:p.Lys643=
NM_001005242.3:c.1797A>G MANE Select	NP_001005242.2:p.Lys599=
NM_004572.4:c.1929A>G	NP_004563.2:p.Lys643=