Canonical Allele Identifier: CA2026360951
Gene: PKP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32796395T= , CM000674.2:g.32796395T= GRCh38
NC_000012.11:g.32949329T= , CM000674.1:g.32949329T= GRCh37
NC_000012.10:g.32840596T= NCBI36
NG_009000.1:g.105452A= , LRG_398:g.105452A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.671-97A=
ENST00000700557.2:n.260-97A=
ENST00000700559.2:c.2168-3664A= ENSP00000515065.2:n.2168-3664A=
ENST00000546498.2:n.855-97A=
ENST00000549461.2:n.660-97A=
ENST00000700555.1:c.599-97A= ENSP00000515062.1:n.599-97A=
ENST00000700556.1:c.639-97A=
ENST00000700557.1:c.179-97A= ENSP00000515064.1:n.179-97A=
ENST00000700558.1:n.382-97A=
ENST00000700559.1:c.1383-3664A=
ENST00000700560.1:n.1383-97A=
ENST00000700561.1:n.1509-97A=
ENST00000070846.11:c.2300-97A= ENSP00000070846.6:n.2300-97A=
ENST00000340811.9:c.2168-97A= MANE Select ENSP00000342800.5:n.2168-97A=
ENST00000070846.10:c.2300-97A= ENSP00000070846.6:n.2300-97A=
ENST00000340811.8:c.2168-97A= ENSP00000342800.4:n.2168-97A=
ENST00000613243.1:c.2300-97A= ENSP00000478295.1:n.2300-97A=
NM_001005242.2:c.2168-97A= NP_001005242.2:n.2168-97A=
NM_004572.3:c.2300-97A= , LRG_398t1:c.2300-97A= NP_004563.2:n.2300-97A=
NM_001005242.3:c.2168-97A= MANE Select NP_001005242.2:n.2168-97A=
NM_004572.4:c.2300-97A= NP_004563.2:n.2300-97A=