Canonical Allele Identifier: CA384359601
Gene: PKP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32802464T>G , CM000674.2:g.32802464T>G GRCh38
NC_000012.11:g.32955398T>G , CM000674.1:g.32955398T>G GRCh37
NC_000012.10:g.32846665T>G NCBI36
NG_009000.1:g.99383A>C , LRG_398:g.99383A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700555.2:n.609A>C
ENST00000700557.2:n.198A>C
ENST00000700559.2:c.2106A>C ENSP00000515065.2:p.Lys702Asn
ENST00000546498.2:n.793A>C
ENST00000549461.2:n.645A>C
ENST00000700555.1:c.537A>C ENSP00000515062.1:p.Lys179Asn
ENST00000700556.1:c.577A>C
ENST00000700557.1:c.117A>C ENSP00000515064.1:p.Lys39Asn
ENST00000700558.1:n.320A>C
ENST00000700559.1:c.1321A>C
ENST00000700560.1:n.1321A>C
ENST00000700561.1:n.1447A>C
ENST00000070846.11:c.2238A>C ENSP00000070846.6:p.Lys746Asn
ENST00000340811.9:c.2106A>C MANE Select ENSP00000342800.5:p.Lys702Asn
ENST00000070846.10:c.2238A>C ENSP00000070846.6:p.Lys746Asn
ENST00000340811.8:c.2106A>C ENSP00000342800.4:p.Lys702Asn
ENST00000549461.1:n.552A>C
ENST00000613243.1:c.2238A>C ENSP00000478295.1:p.Lys746Asn
NM_001005242.2:c.2106A>C NP_001005242.2:p.Lys702Asn
NM_004572.3:c.2238A>C , LRG_398t1:c.2238A>C NP_004563.2:p.Lys746Asn
NM_001005242.3:c.2106A>C MANE Select NP_001005242.2:p.Lys702Asn
NM_004572.4:c.2238A>C NP_004563.2:p.Lys746Asn