Canonical Allele Identifier: CA2522188966
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32796492C>T , CM000674.2:g.32796492C>T GRCh38
NC_000012.11:g.32949426C>T , CM000674.1:g.32949426C>T GRCh37
NC_000012.10:g.32840693C>T NCBI36
NG_009000.1:g.105355G>A , LRG_398:g.105355G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.671-194G>A
ENST00000700557.2:n.260-194G>A
ENST00000700559.2:c.2168-3761G>A ENSP00000515065.2:n.2168-3761G>A
ENST00000546498.2:n.855-194G>A
ENST00000549461.2:n.660-194G>A
ENST00000700555.1:c.599-194G>A ENSP00000515062.1:n.599-194G>A
ENST00000700556.1:c.639-194G>A
ENST00000700557.1:c.179-194G>A ENSP00000515064.1:n.179-194G>A
ENST00000700558.1:n.382-194G>A
ENST00000700559.1:c.1383-3761G>A
ENST00000700560.1:n.1383-194G>A
ENST00000700561.1:n.1509-194G>A
ENST00000070846.11:c.2300-194G>A ENSP00000070846.6:n.2300-194G>A
ENST00000340811.9:c.2168-194G>A MANE Select ENSP00000342800.5:n.2168-194G>A
ENST00000070846.10:c.2300-194G>A ENSP00000070846.6:n.2300-194G>A
ENST00000340811.8:c.2168-194G>A ENSP00000342800.4:n.2168-194G>A
ENST00000613243.1:c.2300-194G>A ENSP00000478295.1:n.2300-194G>A
NM_001005242.2:c.2168-194G>A NP_001005242.2:n.2168-194G>A
NM_004572.3:c.2300-194G>A , LRG_398t1:c.2300-194G>A NP_004563.2:n.2300-194G>A
NM_001005242.3:c.2168-194G>A MANE Select NP_001005242.2:n.2168-194G>A
NM_004572.4:c.2300-194G>A NP_004563.2:n.2300-194G>A