Canonical Allele Identifier: CA1955119199
Gene: KCNJ11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387294T= , CM000673.2:g.17387294T= GRCh38
NC_000011.9:g.17408841T= , CM000673.1:g.17408841T= GRCh37
NC_000011.8:g.17365417T= NCBI36
NG_012446.1:g.6366A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682350.1:c.537A= ENSP00000508090.1:p.Pro179=
ENST00000682764.1:c.537A= ENSP00000506780.1:p.Pro179=
ENST00000339994.5:c.798A= MANE Select ENSP00000345708.4:p.Pro266=
ENST00000339994.4:c.798A= ENSP00000345708.4:p.Pro266=
ENST00000528731.1:c.537A= ENSP00000434755.1:p.Pro179=
NM_000525.3:c.798A= NP_000516.3:p.Pro266=
NM_001166290.1:c.537A= NP_001159762.1:p.Pro179=
XM_006718226.2:c.537A= XP_006718289.1:p.Pro179=
XR_930867.1:n.956A=
XM_006718226.3:c.537A= XP_006718289.1:p.Pro179=
XM_017017680.1:c.537A= XP_016873169.1:p.Pro179=
NM_001166290.2:c.537A= NP_001159762.1:p.Pro179=
NM_001377296.1:c.537A= NP_001364225.1:p.Pro179=
NM_001377297.1:c.537A= NP_001364226.1:p.Pro179=
NM_000525.4:c.798A= MANE Select NP_000516.3:p.Pro266=