Canonical Allele Identifier: CA479176194

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32974422G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32821488G>T , CM000674.2:g.32821488G>T	GRCh38
NC_000012.11:g.32974422G>T , CM000674.1:g.32974422G>T	GRCh37
NC_000012.10:g.32865689G>T	NCBI36
NG_009000.1:g.80359C>A , LRG_398:g.80359C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.384C>A
ENST00000700559.2:c.1881C>A	ENSP00000515065.2:p.Pro627=
ENST00000700563.2:c.1881C>A	ENSP00000515066.2:p.Pro627=
ENST00000546498.2:n.568C>A
ENST00000549461.2:n.420C>A
ENST00000700555.1:c.312C>A	ENSP00000515062.1:p.Pro104=
ENST00000700556.1:c.352C>A
ENST00000700558.1:n.95C>A
ENST00000700559.1:c.1096C>A
ENST00000700560.1:n.1096C>A
ENST00000700561.1:n.1222C>A
ENST00000700562.1:n.419C>A
ENST00000700563.1:c.1835C>A
ENST00000700564.1:n.1885C>A
ENST00000070846.11:c.2013C>A	ENSP00000070846.6:p.Pro671=
ENST00000340811.9:c.1881C>A MANE Select	ENSP00000342800.5:p.Pro627=
ENST00000070846.10:c.2013C>A	ENSP00000070846.6:p.Pro671=
ENST00000340811.8:c.1881C>A	ENSP00000342800.4:p.Pro627=
ENST00000546498.1:n.568C>A
ENST00000549461.1:n.327C>A
ENST00000552612.5:n.302C>A
ENST00000613243.1:c.2013C>A	ENSP00000478295.1:p.Pro671=
NM_001005242.2:c.1881C>A	NP_001005242.2:p.Pro627=
NM_004572.3:c.2013C>A , LRG_398t1:c.2013C>A	NP_004563.2:p.Pro671=
NM_001005242.3:c.1881C>A MANE Select	NP_001005242.2:p.Pro627=
NM_004572.4:c.2013C>A	NP_004563.2:p.Pro671=