Canonical Allele Identifier: CA384362587

Gene: PKP2

Linked Data

• MyVariant Identifiers: chr12:g.32975408A>G (hg19) ; chr12:g.32822474A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32822474A>G , CM000674.2:g.32822474A>G	GRCh38
NC_000012.11:g.32975408A>G , CM000674.1:g.32975408A>G	GRCh37
NC_000012.10:g.32866675A>G	NCBI36
NG_009000.1:g.79373T>C , LRG_398:g.79373T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700555.2:n.342+2T>C
ENST00000700559.2:c.1832T>C	ENSP00000515065.2:p.Val611Ala
ENST00000700563.2:c.1832T>C	ENSP00000515066.2:p.Val611Ala
ENST00000546498.2:n.519T>C
ENST00000700555.1:c.270+2T>C	ENSP00000515062.1:n.270+2T>C
ENST00000700556.1:c.303T>C
ENST00000700559.1:c.1047T>C
ENST00000700560.1:n.1047T>C
ENST00000700561.1:n.1173T>C
ENST00000700563.1:c.1786T>C
ENST00000700564.1:n.1836T>C
ENST00000070846.11:c.1964T>C	ENSP00000070846.6:p.Val655Ala
ENST00000340811.9:c.1832T>C MANE Select	ENSP00000342800.5:p.Val611Ala
ENST00000070846.10:c.1964T>C	ENSP00000070846.6:p.Val655Ala
ENST00000340811.8:c.1832T>C	ENSP00000342800.4:p.Val611Ala
ENST00000546498.1:n.519T>C
ENST00000552612.5:n.253T>C
ENST00000613243.1:c.1964T>C	ENSP00000478295.1:p.Val655Ala
NM_001005242.2:c.1832T>C	NP_001005242.2:p.Val611Ala
NM_004572.3:c.1964T>C , LRG_398t1:c.1964T>C	NP_004563.2:p.Val655Ala
NM_001005242.3:c.1832T>C MANE Select	NP_001005242.2:p.Val611Ala
NM_004572.4:c.1964T>C	NP_004563.2:p.Val655Ala