Canonical Allele Identifier: CA946315253
Gene: PKP2 HGNC NCBI

Linked Data

dbSNP Id: rs1956124809

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32796368A>G , CM000674.2:g.32796368A>G GRCh38
NC_000012.11:g.32949302A>G , CM000674.1:g.32949302A>G GRCh37
NC_000012.10:g.32840569A>G NCBI36
NG_009000.1:g.105479T>C , LRG_398:g.105479T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.671-70T>C
ENST00000700557.2:n.260-70T>C
ENST00000700559.2:c.2168-3637T>C ENSP00000515065.2:n.2168-3637T>C
ENST00000546498.2:n.855-70T>C
ENST00000549461.2:n.660-70T>C
ENST00000700555.1:c.599-70T>C ENSP00000515062.1:n.599-70T>C
ENST00000700556.1:c.639-70T>C
ENST00000700557.1:c.179-70T>C ENSP00000515064.1:n.179-70T>C
ENST00000700558.1:n.382-70T>C
ENST00000700559.1:c.1383-3637T>C
ENST00000700560.1:n.1383-70T>C
ENST00000700561.1:n.1509-70T>C
ENST00000070846.11:c.2300-70T>C ENSP00000070846.6:n.2300-70T>C
ENST00000340811.9:c.2168-70T>C MANE Select ENSP00000342800.5:n.2168-70T>C
ENST00000070846.10:c.2300-70T>C ENSP00000070846.6:n.2300-70T>C
ENST00000340811.8:c.2168-70T>C ENSP00000342800.4:n.2168-70T>C
ENST00000613243.1:c.2300-70T>C ENSP00000478295.1:n.2300-70T>C
NM_001005242.2:c.2168-70T>C NP_001005242.2:n.2168-70T>C
NM_004572.3:c.2300-70T>C , LRG_398t1:c.2300-70T>C NP_004563.2:n.2300-70T>C
NM_001005242.3:c.2168-70T>C MANE Select NP_001005242.2:n.2168-70T>C
NM_004572.4:c.2300-70T>C NP_004563.2:n.2300-70T>C