Canonical Allele Identifier: CA379775455
Gene: KCNJ11 HGNC NCBI

Linked Data

dbSNP Id: rs1211367901
gnomAD v2: 11-17409427-G-A
MyVariant Identifiers: chr11:g.17409427G>A (hg19) chr11:g.17387880G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387880G>A , CM000673.2:g.17387880G>A GRCh38
NC_000011.9:g.17409427G>A , CM000673.1:g.17409427G>A GRCh37
NC_000011.8:g.17366003G>A NCBI36
NG_012446.1:g.5780C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000528992.2:c.-17C>T ENSP00000436479.2:n.-17C>T
ENST00000682350.1:c.-16-34C>T ENSP00000508090.1:n.-16-34C>T
ENST00000682764.1:c.-16-34C>T ENSP00000506780.1:n.-16-34C>T
ENST00000339994.5:c.212C>T MANE Select ENSP00000345708.4:p.Thr71Ile
ENST00000339994.4:c.212C>T ENSP00000345708.4:p.Thr71Ile
ENST00000526912.1:c.-16-34C>T ENSP00000432729.1:n.-16-34C>T
ENST00000528731.1:c.-16-34C>T ENSP00000434755.1:n.-16-34C>T
ENST00000528992.1:c.229C>T
NM_000525.3:c.212C>T NP_000516.3:p.Thr71Ile
NM_001166290.1:c.-16-34C>T NP_001159762.1:n.-16-34C>T
XM_006718226.2:c.-16-34C>T XP_006718289.1:n.-16-34C>T
XR_930867.1:n.370C>T
XM_006718226.3:c.-16-34C>T XP_006718289.1:n.-16-34C>T
XM_017017680.1:c.-16-34C>T XP_016873169.1:n.-16-34C>T
NM_001166290.2:c.-16-34C>T NP_001159762.1:n.-16-34C>T
NM_001377296.1:c.-16-34C>T NP_001364225.1:n.-16-34C>T
NM_001377297.1:c.-16-34C>T NP_001364226.1:n.-16-34C>T
NM_000525.4:c.212C>T MANE Select NP_000516.3:p.Thr71Ile
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