Canonical Allele Identifier: CA479176234

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32975416G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822482G>A , CM000674.2:g.32822482G>A	GRCh38
NC_000012.11:g.32975416G>A , CM000674.1:g.32975416G>A	GRCh37
NC_000012.10:g.32866683G>A	NCBI36
NG_009000.1:g.79365C>T , LRG_398:g.79365C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.336C>T
ENST00000700559.2:c.1824C>T	ENSP00000515065.2:p.Ser608=
ENST00000700563.2:c.1824C>T	ENSP00000515066.2:p.Ser608=
ENST00000546498.2:n.511C>T
ENST00000700555.1:c.264C>T	ENSP00000515062.1:p.Ser88=
ENST00000700556.1:c.295C>T
ENST00000700559.1:c.1039C>T
ENST00000700560.1:n.1039C>T
ENST00000700561.1:n.1165C>T
ENST00000700563.1:c.1778C>T
ENST00000700564.1:n.1828C>T
ENST00000070846.11:c.1956C>T	ENSP00000070846.6:p.Ser652=
ENST00000340811.9:c.1824C>T MANE Select	ENSP00000342800.5:p.Ser608=
ENST00000070846.10:c.1956C>T	ENSP00000070846.6:p.Ser652=
ENST00000340811.8:c.1824C>T	ENSP00000342800.4:p.Ser608=
ENST00000546498.1:n.511C>T
ENST00000552612.5:n.245C>T
ENST00000613243.1:c.1956C>T	ENSP00000478295.1:p.Ser652=
NM_001005242.2:c.1824C>T	NP_001005242.2:p.Ser608=
NM_004572.3:c.1956C>T , LRG_398t1:c.1956C>T	NP_004563.2:p.Ser652=
NM_001005242.3:c.1824C>T MANE Select	NP_001005242.2:p.Ser608=
NM_004572.4:c.1956C>T	NP_004563.2:p.Ser652=