Canonical Allele Identifier: CA10604675
Gene: KCNJ11 HGNC NCBI

Linked Data

dbSNP Id: rs886042779

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387509_17387511del , CM000673.2:g.17387509_17387511del GRCh38
NC_000011.9:g.17409056_17409058del , CM000673.1:g.17409056_17409058del GRCh37
NC_000011.8:g.17365632_17365634del NCBI36
NG_012446.1:g.6152_6154del

Transcript Alleles

HGVS Amino-acid change
ENST00000682350.1:c.323_325del ENSP00000508090.1:p.Arg108del
ENST00000682764.1:c.323_325del ENSP00000506780.1:p.Arg108del
ENST00000339994.5:c.584_586del MANE Select ENSP00000345708.4:p.Arg195del
ENST00000339994.4:c.584_586del ENSP00000345708.4:p.Arg195del
ENST00000526912.1:c.323_325del ENSP00000432729.1:p.Arg108del
ENST00000528731.1:c.323_325del ENSP00000434755.1:p.Arg108del
NM_000525.3:c.584_586del NP_000516.3:p.Arg195del
NM_001166290.1:c.323_325del NP_001159762.1:p.Arg108del
XM_006718226.2:c.323_325del XP_006718289.1:p.Arg108del
XR_930867.1:n.742_744del
XM_006718226.3:c.323_325del XP_006718289.1:p.Arg108del
XM_017017680.1:c.323_325del XP_016873169.1:p.Arg108del
NM_001166290.2:c.323_325del NP_001159762.1:p.Arg108del
NM_001377296.1:c.323_325del NP_001364225.1:p.Arg108del
NM_001377297.1:c.323_325del NP_001364226.1:p.Arg108del
NM_000525.4:c.584_586del MANE Select NP_000516.3:p.Arg195del