Canonical Allele Identifier: CA2499220818
Gene: KCNJ11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1108601

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17388025_17388026delinsCA , CM000673.2:g.17388025_17388026delinsCA GRCh38
NC_000011.9:g.17409572_17409573delinsCA , CM000673.1:g.17409572_17409573delinsCA GRCh37
NC_000011.8:g.17366148_17366149delinsCA NCBI36
NG_012446.1:g.5634_5635delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000528992.2:c.-163_-162delinsTG ENSP00000436479.2:n.-163_-162delinsTG
ENST00000682350.1:c.-16-180_-16-179delinsTG ENSP00000508090.1:n.-16-180_-16-179delins...
ENST00000682764.1:c.-16-180_-16-179delinsTG ENSP00000506780.1:n.-16-180_-16-179delins...
ENST00000339994.5:c.66_67delinsTG MANE Select ENSP00000345708.4:p.Lys23Glu
ENST00000339994.4:c.66_67delinsTG ENSP00000345708.4:p.Lys23Glu
ENST00000526912.1:c.-25_-24delinsTG ENSP00000432729.1:n.-25_-24delinsTG
ENST00000528731.1:c.-16-180_-16-179delinsTG ENSP00000434755.1:n.-16-180_-16-179delins...
ENST00000528992.1:c.83_84delinsTG
NM_000525.3:c.66_67delinsTG NP_000516.3:p.Lys23Glu
NM_001166290.1:c.-16-180_-16-179delinsTG NP_001159762.1:n.-16-180_-16-179delinsTG
XM_006718226.2:c.-16-180_-16-179delinsTG XP_006718289.1:n.-16-180_-16-179delinsTG
XR_930867.1:n.224_225delinsTG
XM_006718226.3:c.-16-180_-16-179delinsTG XP_006718289.1:n.-16-180_-16-179delinsTG
XM_017017680.1:c.-16-180_-16-179delinsTG XP_016873169.1:n.-16-180_-16-179delinsTG
NM_001166290.2:c.-16-180_-16-179delinsTG NP_001159762.1:n.-16-180_-16-179delinsTG
NM_001377296.1:c.-25_-24delinsTG NP_001364225.1:n.-25_-24delinsTG
NM_001377297.1:c.-16-180_-16-179delinsTG NP_001364226.1:n.-16-180_-16-179delinsTG
NM_000525.4:c.66_67delinsTG MANE Select NP_000516.3:p.Lys23Glu