Canonical Allele Identifier: CA935521939
Gene: KCNJ11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17388195_17388196insTAA , CM000673.2:g.17388195_17388196insTAA GRCh38
NC_000011.9:g.17409742_17409743insTAA , CM000673.1:g.17409742_17409743insTAA GRCh37
NC_000011.8:g.17366318_17366319insTAA NCBI36
NG_012446.1:g.5464_5465insTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000528992.2:c.-213-120_-213-119insTTA ENSP00000436479.2:n.-213-120_-213-119insTTA
ENST00000682350.1:c.-16-350_-16-349insTTA ENSP00000508090.1:n.-16-350_-16-349insTTA
ENST00000682764.1:c.-16-350_-16-349insTTA ENSP00000506780.1:n.-16-350_-16-349insTTA
ENST00000339994.5:c.-105_-104insTTA MANE Select ENSP00000345708.4:n.-105_-104insTTA
ENST00000339994.4:c.-105_-104insTTA ENSP00000345708.4:n.-105_-104insTTA
ENST00000526912.1:c.-75-120_-75-119insTTA ENSP00000432729.1:n.-75-120_-75-119insTTA
ENST00000528731.1:c.-16-350_-16-349insTTA ENSP00000434755.1:n.-16-350_-16-349insTTA
ENST00000528992.1:c.33-120_33-119insTTA
NM_000525.3:c.-105_-104insTTA NP_000516.3:n.-105_-104insTTA
NM_001166290.1:c.-16-350_-16-349insTTA NP_001159762.1:n.-16-350_-16-349insTTA
XM_006718226.2:c.-16-350_-16-349insTTA XP_006718289.1:n.-16-350_-16-349insTTA
XR_930867.1:n.54_55insTTA
XM_006718226.3:c.-16-350_-16-349insTTA XP_006718289.1:n.-16-350_-16-349insTTA
XM_017017680.1:c.-16-350_-16-349insTTA XP_016873169.1:n.-16-350_-16-349insTTA
NM_001166290.2:c.-16-350_-16-349insTTA NP_001159762.1:n.-16-350_-16-349insTTA
NM_001377296.1:c.-75-120_-75-119insTTA NP_001364225.1:n.-75-120_-75-119insTTA
NM_001377297.1:c.-16-350_-16-349insTTA NP_001364226.1:n.-16-350_-16-349insTTA
NM_000525.4:c.-105_-104insTTA MANE Select NP_000516.3:n.-105_-104insTTA