Canonical Allele Identifier: CA935521931
Gene: KCNJ11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17388192_17388198del , CM000673.2:g.17388192_17388198del GRCh38
NC_000011.9:g.17409739_17409745del , CM000673.1:g.17409739_17409745del GRCh37
NC_000011.8:g.17366315_17366321del NCBI36
NG_012446.1:g.5462_5468del

Transcript Alleles

HGVS Amino-acid Change
ENST00000528992.2:c.-213-122_-213-116del ENSP00000436479.2:n.-213-122_-213-116del
ENST00000682350.1:c.-16-352_-16-346del ENSP00000508090.1:n.-16-352_-16-346del
ENST00000682764.1:c.-16-352_-16-346del ENSP00000506780.1:n.-16-352_-16-346del
ENST00000339994.5:c.-107_-101del MANE Select ENSP00000345708.4:n.-107_-101del
ENST00000339994.4:c.-107_-101del ENSP00000345708.4:n.-107_-101del
ENST00000526912.1:c.-75-122_-75-116del ENSP00000432729.1:n.-75-122_-75-116del
ENST00000528731.1:c.-16-352_-16-346del ENSP00000434755.1:n.-16-352_-16-346del
ENST00000528992.1:c.33-122_33-116del
NM_000525.3:c.-107_-101del NP_000516.3:n.-107_-101del
NM_001166290.1:c.-16-352_-16-346del NP_001159762.1:n.-16-352_-16-346del
XM_006718226.2:c.-16-352_-16-346del XP_006718289.1:n.-16-352_-16-346del
XR_930867.1:n.52_58del
XM_006718226.3:c.-16-352_-16-346del XP_006718289.1:n.-16-352_-16-346del
XM_017017680.1:c.-16-352_-16-346del XP_016873169.1:n.-16-352_-16-346del
NM_001166290.2:c.-16-352_-16-346del NP_001159762.1:n.-16-352_-16-346del
NM_001377296.1:c.-75-122_-75-116del NP_001364225.1:n.-75-122_-75-116del
NM_001377297.1:c.-16-352_-16-346del NP_001364226.1:n.-16-352_-16-346del
NM_000525.4:c.-107_-101del MANE Select NP_000516.3:n.-107_-101del