Canonical Allele Identifier: CA1955119007
Gene: KCNJ11 HGNC NCBI

Linked Data

dbSNP Id: rs1953565556

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17386889_17386890dup , CM000673.2:g.17386889_17386890dup GRCh38
NC_000011.9:g.17408436_17408437dup , CM000673.1:g.17408436_17408437dup GRCh37
NC_000011.8:g.17365012_17365013dup NCBI36
NG_012446.1:g.6774_6775dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682350.1:c.*33_*34dup ENSP00000508090.1:n.*33_*34dup
ENST00000682764.1:c.*33_*34dup ENSP00000506780.1:n.*33_*34dup
ENST00000339994.5:c.*33_*34dup MANE Select ENSP00000345708.4:n.*33_*34dup
ENST00000339994.4:c.*33_*34dup ENSP00000345708.4:n.*33_*34dup
ENST00000528731.1:c.*33_*34dup ENSP00000434755.1:n.*33_*34dup
NM_000525.3:c.*33_*34dup NP_000516.3:n.*33_*34dup
NM_001166290.1:c.*33_*34dup NP_001159762.1:n.*33_*34dup
XM_006718226.2:c.*33_*34dup XP_006718289.1:n.*33_*34dup
XR_930867.1:n.1364_1365dup
XM_006718226.3:c.*33_*34dup XP_006718289.1:n.*33_*34dup
XM_017017680.1:c.*33_*34dup XP_016873169.1:n.*33_*34dup
NM_001166290.2:c.*33_*34dup NP_001159762.1:n.*33_*34dup
NM_001377296.1:c.*33_*34dup NP_001364225.1:n.*33_*34dup
NM_001377297.1:c.*33_*34dup NP_001364226.1:n.*33_*34dup
NM_000525.4:c.*33_*34dup MANE Select NP_000516.3:n.*33_*34dup