Canonical Allele Identifier: CA2618223110

Gene: PKP2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.32802365C>T , CM000674.2:g.32802365C>T	GRCh38
NC_000012.11:g.32955299C>T , CM000674.1:g.32955299C>T	GRCh37
NC_000012.10:g.32846566C>T	NCBI36
NG_009000.1:g.99482G>A , LRG_398:g.99482G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001005242.3:c.2167+38G>A MANE Select	NP_001005242.2:n.2167+38G>A
ENST00000340811.9:c.2167+38G>A MANE Select	ENSP00000342800.5:n.2167+38G>A
NM_001005242.2:c.2167+38G>A	NP_001005242.2:n.2167+38G>A
NM_004572.3:c.2299+38G>A , LRG_398t1:c.2299+38G>A	NP_004563.2:n.2299+38G>A
NM_004572.4:c.2299+38G>A	NP_004563.2:n.2299+38G>A
ENST00000070846.10:c.2299+38G>A	ENSP00000070846.6:n.2299+38G>A
ENST00000070846.11:c.2299+38G>A	ENSP00000070846.6:n.2299+38G>A
ENST00000340811.8:c.2167+38G>A	ENSP00000342800.4:n.2167+38G>A
ENST00000546498.2:n.854+38G>A
ENST00000549461.2:n.659+85G>A
ENST00000613243.1:c.2299+38G>A	ENSP00000478295.1:n.2299+38G>A
ENST00000700555.1:c.598+38G>A	ENSP00000515062.1:n.598+38G>A
ENST00000700555.2:n.670+38G>A
ENST00000700556.1:c.638+38G>A
ENST00000700557.1:c.178+38G>A	ENSP00000515064.1:n.178+38G>A
ENST00000700557.2:n.259+38G>A
ENST00000700558.1:n.381+38G>A
ENST00000700559.1:c.1382+38G>A
ENST00000700559.2:c.2167+38G>A	ENSP00000515065.2:n.2167+38G>A
ENST00000700560.1:n.1382+38G>A
ENST00000700561.1:n.1508+38G>A