Canonical Allele Identifier: CA1955119502
Gene: KCNJ11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17388043G= , CM000673.2:g.17388043G= GRCh38
NC_000011.9:g.17409590G= , CM000673.1:g.17409590G= GRCh37
NC_000011.8:g.17366166G= NCBI36
NG_012446.1:g.5617C=

Transcript Alleles

HGVS Amino-acid change
ENST00000528992.2:c.-180C= ENSP00000436479.2:n.-180C=
ENST00000682350.1:c.-16-197C= ENSP00000508090.1:n.-16-197C=
ENST00000682764.1:c.-16-197C= ENSP00000506780.1:n.-16-197C=
ENST00000339994.5:c.49C= MANE Select ENSP00000345708.4:p.Leu17=
ENST00000339994.4:c.49C= ENSP00000345708.4:p.Leu17=
ENST00000526912.1:c.-42C= ENSP00000432729.1:n.-42C=
ENST00000528731.1:c.-16-197C= ENSP00000434755.1:n.-16-197C=
ENST00000528992.1:c.66C=
NM_000525.3:c.49C= NP_000516.3:p.Leu17=
NM_001166290.1:c.-16-197C= NP_001159762.1:n.-16-197C=
XM_006718226.2:c.-16-197C= XP_006718289.1:n.-16-197C=
XR_930867.1:n.207C=
XM_006718226.3:c.-16-197C= XP_006718289.1:n.-16-197C=
XM_017017680.1:c.-16-197C= XP_016873169.1:n.-16-197C=
NM_001166290.2:c.-16-197C= NP_001159762.1:n.-16-197C=
NM_001377296.1:c.-42C= NP_001364225.1:n.-42C=
NM_001377297.1:c.-16-197C= NP_001364226.1:n.-16-197C=
NM_000525.4:c.49C= MANE Select NP_000516.3:p.Leu17=