Canonical Allele Identifier: CA3003288829
Gene: KCNJ11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387334dup , CM000673.2:g.17387334dup GRCh38
NC_000011.9:g.17408881dup , CM000673.1:g.17408881dup GRCh37
NC_000011.8:g.17365457dup NCBI36
NG_012446.1:g.6329dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682350.1:c.500dup ENSP00000508090.1:p.Leu168AlafsTer8
ENST00000682764.1:c.500dup ENSP00000506780.1:p.Leu168AlafsTer8
ENST00000339994.5:c.761dup MANE Select ENSP00000345708.4:p.Leu255AlafsTer8
ENST00000339994.4:c.761dup ENSP00000345708.4:p.Leu255AlafsTer8
ENST00000528731.1:c.500dup ENSP00000434755.1:p.Leu168AlafsTer8
NM_000525.3:c.761dup NP_000516.3:p.Leu255AlafsTer8
NM_001166290.1:c.500dup NP_001159762.1:p.Leu168AlafsTer8
XM_006718226.2:c.500dup XP_006718289.1:p.Leu168AlafsTer8
XR_930867.1:n.919dup
XM_006718226.3:c.500dup XP_006718289.1:p.Leu168AlafsTer8
XM_017017680.1:c.500dup XP_016873169.1:p.Leu168AlafsTer8
NM_001166290.2:c.500dup NP_001159762.1:p.Leu168AlafsTer8
NM_001377296.1:c.500dup NP_001364225.1:p.Leu168AlafsTer8
NM_001377297.1:c.500dup NP_001364226.1:p.Leu168AlafsTer8
NM_000525.4:c.761dup MANE Select NP_000516.3:p.Leu255AlafsTer8