Canonical Allele Identifier: CA214110
Gene: KCNJ11 HGNC NCBI

Linked Data

ClinVar Variation Id: 36432
dbSNP Id: rs193922564

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17388038T>C , CM000673.2:g.17388038T>C GRCh38
NC_000011.9:g.17409585T>C , CM000673.1:g.17409585T>C GRCh37
NC_000011.8:g.17366161T>C NCBI36
NG_012446.1:g.5622A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000528992.2:c.-175A>G ENSP00000436479.2:n.-175A>G
ENST00000682350.1:c.-16-192A>G ENSP00000508090.1:n.-16-192A>G
ENST00000682764.1:c.-16-192A>G ENSP00000506780.1:n.-16-192A>G
ENST00000339994.5:c.54A>G MANE Select ENSP00000345708.4:p.Ala18=
ENST00000339994.4:c.54A>G ENSP00000345708.4:p.Ala18=
ENST00000526912.1:c.-37A>G ENSP00000432729.1:n.-37A>G
ENST00000528731.1:c.-16-192A>G ENSP00000434755.1:n.-16-192A>G
ENST00000528992.1:c.71A>G
NM_000525.3:c.54A>G NP_000516.3:p.Ala18=
NM_001166290.1:c.-16-192A>G NP_001159762.1:n.-16-192A>G
XM_006718226.2:c.-16-192A>G XP_006718289.1:n.-16-192A>G
XR_930867.1:n.212A>G
XM_006718226.3:c.-16-192A>G XP_006718289.1:n.-16-192A>G
XM_017017680.1:c.-16-192A>G XP_016873169.1:n.-16-192A>G
NM_001166290.2:c.-16-192A>G NP_001159762.1:n.-16-192A>G
NM_001377296.1:c.-37A>G NP_001364225.1:n.-37A>G
NM_001377297.1:c.-16-192A>G NP_001364226.1:n.-16-192A>G
NM_000525.4:c.54A>G MANE Select NP_000516.3:p.Ala18=