Canonical Allele Identifier: CA384362573
Gene: PKP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32822471T>G , CM000674.2:g.32822471T>G GRCh38
NC_000012.11:g.32975405T>G , CM000674.1:g.32975405T>G GRCh37
NC_000012.10:g.32866672T>G NCBI36
NG_009000.1:g.79376A>C , LRG_398:g.79376A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.342+5A>C
ENST00000700559.2:c.1835A>C ENSP00000515065.2:p.Lys612Thr
ENST00000700563.2:c.1835A>C ENSP00000515066.2:p.Lys612Thr
ENST00000546498.2:n.522A>C
ENST00000700555.1:c.270+5A>C ENSP00000515062.1:n.270+5A>C
ENST00000700556.1:c.306A>C
ENST00000700559.1:c.1050A>C
ENST00000700560.1:n.1050A>C
ENST00000700561.1:n.1176A>C
ENST00000700563.1:c.1789A>C
ENST00000700564.1:n.1839A>C
ENST00000070846.11:c.1967A>C ENSP00000070846.6:p.Lys656Thr
ENST00000340811.9:c.1835A>C MANE Select ENSP00000342800.5:p.Lys612Thr
ENST00000070846.10:c.1967A>C ENSP00000070846.6:p.Lys656Thr
ENST00000340811.8:c.1835A>C ENSP00000342800.4:p.Lys612Thr
ENST00000546498.1:n.522A>C
ENST00000552612.5:n.256A>C
ENST00000613243.1:c.1967A>C ENSP00000478295.1:p.Lys656Thr
NM_001005242.2:c.1835A>C NP_001005242.2:p.Lys612Thr
NM_004572.3:c.1967A>C , LRG_398t1:c.1967A>C NP_004563.2:p.Lys656Thr
NM_001005242.3:c.1835A>C MANE Select NP_001005242.2:p.Lys612Thr
NM_004572.4:c.1967A>C NP_004563.2:p.Lys656Thr