Canonical Allele Identifier: CA379771372
Gene: KCNJ11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387389G>T , CM000673.2:g.17387389G>T GRCh38
NC_000011.9:g.17408936G>T , CM000673.1:g.17408936G>T GRCh37
NC_000011.8:g.17365512G>T NCBI36
NG_012446.1:g.6271C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682350.1:c.442C>A ENSP00000508090.1:p.Gln148Lys
ENST00000682764.1:c.442C>A ENSP00000506780.1:p.Gln148Lys
ENST00000339994.5:c.703C>A MANE Select ENSP00000345708.4:p.Gln235Lys
ENST00000339994.4:c.703C>A ENSP00000345708.4:p.Gln235Lys
ENST00000526912.1:c.442C>A ENSP00000432729.1:p.Gln148Lys
ENST00000528731.1:c.442C>A ENSP00000434755.1:p.Gln148Lys
NM_000525.3:c.703C>A NP_000516.3:p.Gln235Lys
NM_001166290.1:c.442C>A NP_001159762.1:p.Gln148Lys
XM_006718226.2:c.442C>A XP_006718289.1:p.Gln148Lys
XR_930867.1:n.861C>A
XM_006718226.3:c.442C>A XP_006718289.1:p.Gln148Lys
XM_017017680.1:c.442C>A XP_016873169.1:p.Gln148Lys
NM_001166290.2:c.442C>A NP_001159762.1:p.Gln148Lys
NM_001377296.1:c.442C>A NP_001364225.1:p.Gln148Lys
NM_001377297.1:c.442C>A NP_001364226.1:p.Gln148Lys
NM_000525.4:c.703C>A MANE Select NP_000516.3:p.Gln235Lys