Canonical Allele Identifier: CA3003288855
Gene: KCNJ11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387340del , CM000673.2:g.17387340del GRCh38
NC_000011.9:g.17408887del , CM000673.1:g.17408887del GRCh37
NC_000011.8:g.17365463del NCBI36
NG_012446.1:g.6320del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682350.1:c.491del ENSP00000508090.1:p.Leu164ArgfsTer5
ENST00000682764.1:c.491del ENSP00000506780.1:p.Leu164ArgfsTer5
ENST00000339994.5:c.752del MANE Select ENSP00000345708.4:p.Leu251ArgfsTer5
ENST00000339994.4:c.752del ENSP00000345708.4:p.Leu251ArgfsTer5
ENST00000528731.1:c.491del ENSP00000434755.1:p.Leu164ArgfsTer5
NM_000525.3:c.752del NP_000516.3:p.Leu251ArgfsTer5
NM_001166290.1:c.491del NP_001159762.1:p.Leu164ArgfsTer5
XM_006718226.2:c.491del XP_006718289.1:p.Leu164ArgfsTer5
XR_930867.1:n.910del
XM_006718226.3:c.491del XP_006718289.1:p.Leu164ArgfsTer5
XM_017017680.1:c.491del XP_016873169.1:p.Leu164ArgfsTer5
NM_001166290.2:c.491del NP_001159762.1:p.Leu164ArgfsTer5
NM_001377296.1:c.491del NP_001364225.1:p.Leu164ArgfsTer5
NM_001377297.1:c.491del NP_001364226.1:p.Leu164ArgfsTer5
NM_000525.4:c.752del MANE Select NP_000516.3:p.Leu251ArgfsTer5