Canonical Allele Identifier: CA384359541
Gene: PKP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32802459G>T , CM000674.2:g.32802459G>T GRCh38
NC_000012.11:g.32955393G>T , CM000674.1:g.32955393G>T GRCh37
NC_000012.10:g.32846660G>T NCBI36
NG_009000.1:g.99388C>A , LRG_398:g.99388C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000700555.2:n.614C>A
ENST00000700557.2:n.203C>A
ENST00000700559.2:c.2111C>A ENSP00000515065.2:p.Thr704Lys
ENST00000546498.2:n.798C>A
ENST00000549461.2:n.650C>A
ENST00000700555.1:c.542C>A ENSP00000515062.1:p.Thr181Lys
ENST00000700556.1:c.582C>A
ENST00000700557.1:c.122C>A ENSP00000515064.1:p.Thr41Lys
ENST00000700558.1:n.325C>A
ENST00000700559.1:c.1326C>A
ENST00000700560.1:n.1326C>A
ENST00000700561.1:n.1452C>A
ENST00000070846.11:c.2243C>A ENSP00000070846.6:p.Thr748Lys
ENST00000340811.9:c.2111C>A MANE Select ENSP00000342800.5:p.Thr704Lys
ENST00000070846.10:c.2243C>A ENSP00000070846.6:p.Thr748Lys
ENST00000340811.8:c.2111C>A ENSP00000342800.4:p.Thr704Lys
ENST00000549461.1:n.557C>A
ENST00000613243.1:c.2243C>A ENSP00000478295.1:p.Thr748Lys
NM_001005242.2:c.2111C>A NP_001005242.2:p.Thr704Lys
NM_004572.3:c.2243C>A , LRG_398t1:c.2243C>A NP_004563.2:p.Thr748Lys
NM_001005242.3:c.2111C>A MANE Select NP_001005242.2:p.Thr704Lys
NM_004572.4:c.2243C>A NP_004563.2:p.Thr748Lys