Canonical Allele Identifier: CA2574767896
Gene: KCNJ11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17386891_17386892insGAC , CM000673.2:g.17386891_17386892insGAC GRCh38
NC_000011.9:g.17408438_17408439insGAC , CM000673.1:g.17408438_17408439insGAC GRCh37
NC_000011.8:g.17365014_17365015insGAC NCBI36
NG_012446.1:g.6768_6769insGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000682350.1:c.*27_*28insGTC ENSP00000508090.1:n.*27_*28insGTC
ENST00000682764.1:c.*27_*28insGTC ENSP00000506780.1:n.*27_*28insGTC
ENST00000339994.5:c.*27_*28insGTC MANE Select ENSP00000345708.4:n.*27_*28insGTC
ENST00000339994.4:c.*27_*28insGTC ENSP00000345708.4:n.*27_*28insGTC
ENST00000528731.1:c.*27_*28insGTC ENSP00000434755.1:n.*27_*28insGTC
NM_000525.3:c.*27_*28insGTC NP_000516.3:n.*27_*28insGTC
NM_001166290.1:c.*27_*28insGTC NP_001159762.1:n.*27_*28insGTC
XM_006718226.2:c.*27_*28insGTC XP_006718289.1:n.*27_*28insGTC
XR_930867.1:n.1358_1359insGTC
XM_006718226.3:c.*27_*28insGTC XP_006718289.1:n.*27_*28insGTC
XM_017017680.1:c.*27_*28insGTC XP_016873169.1:n.*27_*28insGTC
NM_001166290.2:c.*27_*28insGTC NP_001159762.1:n.*27_*28insGTC
NM_001377296.1:c.*27_*28insGTC NP_001364225.1:n.*27_*28insGTC
NM_001377297.1:c.*27_*28insGTC NP_001364226.1:n.*27_*28insGTC
NM_000525.4:c.*27_*28insGTC MANE Select NP_000516.3:n.*27_*28insGTC