Canonical Allele Identifier: CA1955119546
Gene: KCNJ11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17388121_17388134delinsCCCCATCGGAGGCA , CM000673.2:g.17388121_17388134delinsCCCCATCGGAGGCA GRCh38
NC_000011.9:g.17409668_17409681delinsCCCCATCGGAGGCA , CM000673.1:g.17409668_17409681delinsCCCCATCGGAGGCA GRCh37
NC_000011.8:g.17366244_17366257delinsCCCCATCGGAGGCA NCBI36
NG_012446.1:g.5526_5539delinsTGCCTCCGATGGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000528992.2:c.-213-58_-213-45delinsTGCCTCCGATGGGG ENSP00000436479.2:n.-213-58_-213-45delins...
ENST00000682350.1:c.-16-288_-16-275delinsTGCCTCCGATGGGG ENSP00000508090.1:n.-16-288_-16-275delins...
ENST00000682764.1:c.-16-288_-16-275delinsTGCCTCCGATGGGG ENSP00000506780.1:n.-16-288_-16-275delins...
ENST00000339994.5:c.-43_-30delinsTGCCTCCGATGGGG MANE Select ENSP00000345708.4:n.-43_-30delinsTGCCTCCG...
ENST00000339994.4:c.-43_-30delinsTGCCTCCGATGGGG ENSP00000345708.4:n.-43_-30delinsTGCCTCCG...
ENST00000526912.1:c.-75-58_-75-45delinsTGCCTCCGATGGGG ENSP00000432729.1:n.-75-58_-75-45delinsTG...
ENST00000528731.1:c.-16-288_-16-275delinsTGCCTCCGATGGGG ENSP00000434755.1:n.-16-288_-16-275delins...
ENST00000528992.1:c.33-58_33-45delinsTGCCTCCGATGGGG
NM_000525.3:c.-43_-30delinsTGCCTCCGATGGGG NP_000516.3:n.-43_-30delinsTGCCTCCGATGGGG...
NM_001166290.1:c.-16-288_-16-275delinsTGCCTCCGATGGGG NP_001159762.1:n.-16-288_-16-275delinsTGC...
XM_006718226.2:c.-16-288_-16-275delinsTGCCTCCGATGGGG XP_006718289.1:n.-16-288_-16-275delinsTGC...
XR_930867.1:n.116_129delinsTGCCTCCGATGGGG
XM_006718226.3:c.-16-288_-16-275delinsTGCCTCCGATGGGG XP_006718289.1:n.-16-288_-16-275delinsTGC...
XM_017017680.1:c.-16-288_-16-275delinsTGCCTCCGATGGGG XP_016873169.1:n.-16-288_-16-275delinsTGC...
NM_001166290.2:c.-16-288_-16-275delinsTGCCTCCGATGGGG NP_001159762.1:n.-16-288_-16-275delinsTGC...
NM_001377296.1:c.-75-58_-75-45delinsTGCCTCCGATGGGG NP_001364225.1:n.-75-58_-75-45delinsTGCCT...
NM_001377297.1:c.-16-288_-16-275delinsTGCCTCCGATGGGG NP_001364226.1:n.-16-288_-16-275delinsTGC...
NM_000525.4:c.-43_-30delinsTGCCTCCGATGGGG MANE Select NP_000516.3:n.-43_-30delinsTGCCTCCGATGGGG...