Canonical Allele Identifier: CA5902225
Gene: KCNJ11 HGNC NCBI

Linked Data

dbSNP Id: rs74339576

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387190C>A , CM000673.2:g.17387190C>A GRCh38
NC_000011.9:g.17408737C>A , CM000673.1:g.17408737C>A GRCh37
NC_000011.8:g.17365313C>A NCBI36
NG_012446.1:g.6470G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682350.1:c.641G>T ENSP00000508090.1:p.Arg214Leu
ENST00000682764.1:c.641G>T ENSP00000506780.1:p.Arg214Leu
ENST00000339994.5:c.902G>T MANE Select ENSP00000345708.4:p.Arg301Leu
ENST00000339994.4:c.902G>T ENSP00000345708.4:p.Arg301Leu
ENST00000528731.1:c.641G>T ENSP00000434755.1:p.Arg214Leu
NM_000525.3:c.902G>T NP_000516.3:p.Arg301Leu
NM_001166290.1:c.641G>T NP_001159762.1:p.Arg214Leu
XM_006718226.2:c.641G>T XP_006718289.1:p.Arg214Leu
XR_930867.1:n.1060G>T
XM_006718226.3:c.641G>T XP_006718289.1:p.Arg214Leu
XM_017017680.1:c.641G>T XP_016873169.1:p.Arg214Leu
NM_001166290.2:c.641G>T NP_001159762.1:p.Arg214Leu
NM_001377296.1:c.641G>T NP_001364225.1:p.Arg214Leu
NM_001377297.1:c.641G>T NP_001364226.1:p.Arg214Leu
NM_000525.4:c.902G>T MANE Select NP_000516.3:p.Arg301Leu