Canonical Allele Identifier: CA2616775473
Gene: KCNJ5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128912053_128912063del , CM000673.2:g.128912053_128912063del GRCh38
NC_000011.9:g.128781948_128781958del , CM000673.1:g.128781948_128781958del GRCh37
NC_000011.8:g.128287158_128287168del NCBI36
NG_023406.2:g.25636_25646del , LRG_333:g.25636_25646del

Transcript Alleles

HGVS Amino-acid Change
ENST00000529694.6:c.780_790del MANE Select ENSP00000433295.1:p.Phe261ArgfsTer15
ENST00000338350.4:c.780_790del ENSP00000339960.4:p.Phe261ArgfsTer15
ENST00000529694.5:c.780_790del ENSP00000433295.1:p.Phe261ArgfsTer15
ENST00000533599.1:c.780_790del ENSP00000434266.1:p.Phe261ArgfsTer15
NM_000890.3:c.780_790del , LRG_333t1:c.780_790del NP_000881.3:p.Phe261ArgfsTer15
XM_011542809.1:c.780_790del XP_011541111.1:p.Phe261ArgfsTer15
XM_011542810.1:c.780_790del XP_011541112.1:p.Phe261ArgfsTer15
NM_000890.4:c.780_790del NP_000881.3:p.Phe261ArgfsTer15
NM_001354169.1:c.780_790del NP_001341098.1:p.Phe261ArgfsTer15
XM_011542809.2:c.780_790del XP_011541111.1:p.Phe261ArgfsTer15
XM_011542810.3:c.780_790del XP_011541112.1:p.Phe261ArgfsTer15
NM_000890.5:c.780_790del MANE Select NP_000881.3:p.Phe261ArgfsTer15
NM_001354169.2:c.780_790del NP_001341098.1:p.Phe261ArgfsTer15