Canonical Allele Identifier: CA2795079910
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32796299_32796300insAA , CM000674.2:g.32796299_32796300insAA GRCh38
NC_000012.11:g.32949233_32949234insAA , CM000674.1:g.32949233_32949234insAA GRCh37
NC_000012.10:g.32840500_32840501insAA NCBI36
NG_009000.1:g.105547_105548insTT , LRG_398:g.105547_105548insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.671-2_671-1insTT
ENST00000700557.2:n.260-2_260-1insTT
ENST00000700559.2:c.2168-3569_2168-3568insTT ENSP00000515065.2:n.2168-3569_2168-3568insTT
ENST00000546498.2:n.855-2_855-1insTT
ENST00000549461.2:n.660-2_660-1insTT
ENST00000700555.1:c.599-2_599-1insTT ENSP00000515062.1:n.599-2_599-1insTT
ENST00000700556.1:c.639-2_639-1insTT
ENST00000700557.1:c.179-2_179-1insTT ENSP00000515064.1:n.179-2_179-1insTT
ENST00000700558.1:n.382-2_382-1insTT
ENST00000700559.1:c.1383-3569_1383-3568insTT
ENST00000700560.1:n.1383-2_1383-1insTT
ENST00000700561.1:n.1509-2_1509-1insTT
ENST00000070846.11:c.2300-2_2300-1insTT ENSP00000070846.6:n.2300-2_2300-1insTT
ENST00000340811.9:c.2168-2_2168-1insTT MANE Select ENSP00000342800.5:n.2168-2_2168-1insTT
ENST00000070846.10:c.2300-2_2300-1insTT ENSP00000070846.6:n.2300-2_2300-1insTT
ENST00000340811.8:c.2168-2_2168-1insTT ENSP00000342800.4:n.2168-2_2168-1insTT
ENST00000613243.1:c.2300-2_2300-1insTT ENSP00000478295.1:n.2300-2_2300-1insTT
NM_001005242.2:c.2168-2_2168-1insTT NP_001005242.2:n.2168-2_2168-1insTT
NM_004572.3:c.2300-2_2300-1insTT , LRG_398t1:c.2300-2_2300-1insTT NP_004563.2:n.2300-2_2300-1insTT
NM_001005242.3:c.2168-2_2168-1insTT MANE Select NP_001005242.2:n.2168-2_2168-1insTT
NM_004572.4:c.2300-2_2300-1insTT NP_004563.2:n.2300-2_2300-1insTT