Canonical Allele Identifier: CA2695213382
Gene: KCNJ11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387086del , CM000673.2:g.17387086del GRCh38
NC_000011.9:g.17408633del , CM000673.1:g.17408633del GRCh37
NC_000011.8:g.17365209del NCBI36
NG_012446.1:g.6574del

Transcript Alleles

HGVS Amino-acid change
ENST00000682350.1:c.745del ENSP00000508090.1:p.Thr249ProfsTer24
ENST00000682764.1:c.745del ENSP00000506780.1:p.Thr249ProfsTer24
ENST00000339994.5:c.1006del MANE Select ENSP00000345708.4:p.Thr336ProfsTer24
ENST00000339994.4:c.1006del ENSP00000345708.4:p.Thr336ProfsTer24
ENST00000528731.1:c.745del ENSP00000434755.1:p.Thr249ProfsTer24
NM_000525.3:c.1006del NP_000516.3:p.Thr336ProfsTer24
NM_001166290.1:c.745del NP_001159762.1:p.Thr249ProfsTer24
XM_006718226.2:c.745del XP_006718289.1:p.Thr249ProfsTer24
XR_930867.1:n.1164del
XM_006718226.3:c.745del XP_006718289.1:p.Thr249ProfsTer24
XM_017017680.1:c.745del XP_016873169.1:p.Thr249ProfsTer24
NM_001166290.2:c.745del NP_001159762.1:p.Thr249ProfsTer24
NM_001377296.1:c.745del NP_001364225.1:p.Thr249ProfsTer24
NM_001377297.1:c.745del NP_001364226.1:p.Thr249ProfsTer24
NM_000525.4:c.1006del MANE Select NP_000516.3:p.Thr336ProfsTer24