Canonical Allele Identifier: CA2695213384
Gene: KCNJ11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387277_17387278insA , CM000673.2:g.17387277_17387278insA GRCh38
NC_000011.9:g.17408824_17408825insA , CM000673.1:g.17408824_17408825insA GRCh37
NC_000011.8:g.17365400_17365401insA NCBI36
NG_012446.1:g.6382_6383insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682350.1:c.553_554insT ENSP00000508090.1:p.Pro185LeufsTer?
ENST00000682764.1:c.553_554insT ENSP00000506780.1:p.Pro185LeufsTer?
ENST00000339994.5:c.814_815insT MANE Select ENSP00000345708.4:p.Pro272LeufsTer?
ENST00000339994.4:c.814_815insT ENSP00000345708.4:p.Pro272LeufsTer?
ENST00000528731.1:c.553_554insT ENSP00000434755.1:p.Pro185LeufsTer?
NM_000525.3:c.814_815insT NP_000516.3:p.Pro272LeufsTer?
NM_001166290.1:c.553_554insT NP_001159762.1:p.Pro185LeufsTer?
XM_006718226.2:c.553_554insT XP_006718289.1:p.Pro185LeufsTer?
XR_930867.1:n.972_973insT
XM_006718226.3:c.553_554insT XP_006718289.1:p.Pro185LeufsTer?
XM_017017680.1:c.553_554insT XP_016873169.1:p.Pro185LeufsTer?
NM_001166290.2:c.553_554insT NP_001159762.1:p.Pro185LeufsTer?
NM_001377296.1:c.553_554insT NP_001364225.1:p.Pro185LeufsTer?
NM_001377297.1:c.553_554insT NP_001364226.1:p.Pro185LeufsTer?
NM_000525.4:c.814_815insT MANE Select NP_000516.3:p.Pro272LeufsTer?