Canonical Allele Identifier: CA1955119495
Gene: KCNJ11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17388030G= , CM000673.2:g.17388030G= GRCh38
NC_000011.9:g.17409577G= , CM000673.1:g.17409577G= GRCh37
NC_000011.8:g.17366153G= NCBI36
NG_012446.1:g.5630C=

Transcript Alleles

HGVS Amino-acid change
ENST00000528992.2:c.-167C= ENSP00000436479.2:n.-167C=
ENST00000682350.1:c.-16-184C= ENSP00000508090.1:n.-16-184C=
ENST00000682764.1:c.-16-184C= ENSP00000506780.1:n.-16-184C=
ENST00000339994.5:c.62C= MANE Select ENSP00000345708.4:p.Pro21=
ENST00000339994.4:c.62C= ENSP00000345708.4:p.Pro21=
ENST00000526912.1:c.-29C= ENSP00000432729.1:n.-29C=
ENST00000528731.1:c.-16-184C= ENSP00000434755.1:n.-16-184C=
ENST00000528992.1:c.79C=
NM_000525.3:c.62C= NP_000516.3:p.Pro21=
NM_001166290.1:c.-16-184C= NP_001159762.1:n.-16-184C=
XM_006718226.2:c.-16-184C= XP_006718289.1:n.-16-184C=
XR_930867.1:n.220C=
XM_006718226.3:c.-16-184C= XP_006718289.1:n.-16-184C=
XM_017017680.1:c.-16-184C= XP_016873169.1:n.-16-184C=
NM_001166290.2:c.-16-184C= NP_001159762.1:n.-16-184C=
NM_001377296.1:c.-29C= NP_001364225.1:n.-29C=
NM_001377297.1:c.-16-184C= NP_001364226.1:n.-16-184C=
NM_000525.4:c.62C= MANE Select NP_000516.3:p.Pro21=