Canonical Allele Identifier: CA384361748
Gene: PKP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32821422A>T , CM000674.2:g.32821422A>T GRCh38
NC_000012.11:g.32974356A>T , CM000674.1:g.32974356A>T GRCh37
NC_000012.10:g.32865623A>T NCBI36
NG_009000.1:g.80425T>A , LRG_398:g.80425T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000700555.2:n.450T>A
ENST00000700559.2:c.1947T>A ENSP00000515065.2:p.Ser649Arg
ENST00000700563.2:c.1947T>A ENSP00000515066.2:p.Ser649Arg
ENST00000546498.2:n.634T>A
ENST00000549461.2:n.486T>A
ENST00000700555.1:c.378T>A ENSP00000515062.1:p.Ser126Arg
ENST00000700556.1:c.418T>A
ENST00000700558.1:n.161T>A
ENST00000700559.1:c.1162T>A
ENST00000700560.1:n.1162T>A
ENST00000700561.1:n.1288T>A
ENST00000700562.1:n.485T>A
ENST00000700563.1:c.1901T>A
ENST00000700564.1:n.1951T>A
ENST00000070846.11:c.2079T>A ENSP00000070846.6:p.Ser693Arg
ENST00000340811.9:c.1947T>A MANE Select ENSP00000342800.5:p.Ser649Arg
ENST00000070846.10:c.2079T>A ENSP00000070846.6:p.Ser693Arg
ENST00000340811.8:c.1947T>A ENSP00000342800.4:p.Ser649Arg
ENST00000549461.1:n.393T>A
ENST00000552612.5:n.368T>A
ENST00000613243.1:c.2079T>A ENSP00000478295.1:p.Ser693Arg
NM_001005242.2:c.1947T>A NP_001005242.2:p.Ser649Arg
NM_004572.3:c.2079T>A , LRG_398t1:c.2079T>A NP_004563.2:p.Ser693Arg
NM_001005242.3:c.1947T>A MANE Select NP_001005242.2:p.Ser649Arg
NM_004572.4:c.2079T>A NP_004563.2:p.Ser693Arg