Canonical Allele Identifier: CA384359372
Gene: PKP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32802437A>T , CM000674.2:g.32802437A>T GRCh38
NC_000012.11:g.32955371A>T , CM000674.1:g.32955371A>T GRCh37
NC_000012.10:g.32846638A>T NCBI36
NG_009000.1:g.99410T>A , LRG_398:g.99410T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.636T>A
ENST00000700557.2:n.225T>A
ENST00000700559.2:c.2133T>A ENSP00000515065.2:p.Asn711Lys
ENST00000546498.2:n.820T>A
ENST00000549461.2:n.659+13T>A
ENST00000700555.1:c.564T>A ENSP00000515062.1:p.Asn188Lys
ENST00000700556.1:c.604T>A
ENST00000700557.1:c.144T>A ENSP00000515064.1:p.Asn48Lys
ENST00000700558.1:n.347T>A
ENST00000700559.1:c.1348T>A
ENST00000700560.1:n.1348T>A
ENST00000700561.1:n.1474T>A
ENST00000070846.11:c.2265T>A ENSP00000070846.6:p.Asn755Lys
ENST00000340811.9:c.2133T>A MANE Select ENSP00000342800.5:p.Asn711Lys
ENST00000070846.10:c.2265T>A ENSP00000070846.6:p.Asn755Lys
ENST00000340811.8:c.2133T>A ENSP00000342800.4:p.Asn711Lys
ENST00000613243.1:c.2265T>A ENSP00000478295.1:p.Asn755Lys
NM_001005242.2:c.2133T>A NP_001005242.2:p.Asn711Lys
NM_004572.3:c.2265T>A , LRG_398t1:c.2265T>A NP_004563.2:p.Asn755Lys
NM_001005242.3:c.2133T>A MANE Select NP_001005242.2:p.Asn711Lys
NM_004572.4:c.2265T>A NP_004563.2:p.Asn755Lys