Canonical Allele Identifier: CA1955119285

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387505_17387508delinsAGGC , CM000673.2:g.17387505_17387508delinsAGGC	GRCh38
NC_000011.9:g.17409052_17409055delinsAGGC , CM000673.1:g.17409052_17409055delinsAGGC	GRCh37
NC_000011.8:g.17365628_17365631delinsAGGC	NCBI36
NG_012446.1:g.6152_6155delinsGCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000682350.1:c.323_326delinsGCCT	ENSP00000508090.1:p.Arg108=
ENST00000682764.1:c.323_326delinsGCCT	ENSP00000506780.1:p.Arg108=
ENST00000339994.5:c.584_587delinsGCCT MANE Select	ENSP00000345708.4:p.Arg195=
ENST00000339994.4:c.584_587delinsGCCT	ENSP00000345708.4:p.Arg195=
ENST00000526912.1:c.323_326delinsGCCT	ENSP00000432729.1:p.Arg108=
ENST00000528731.1:c.323_326delinsGCCT	ENSP00000434755.1:p.Arg108=
NM_000525.3:c.584_587delinsGCCT	NP_000516.3:p.Arg195=
NM_001166290.1:c.323_326delinsGCCT	NP_001159762.1:p.Arg108=
XM_006718226.2:c.323_326delinsGCCT	XP_006718289.1:p.Arg108=
XR_930867.1:n.742_745delinsGCCT
XM_006718226.3:c.323_326delinsGCCT	XP_006718289.1:p.Arg108=
XM_017017680.1:c.323_326delinsGCCT	XP_016873169.1:p.Arg108=
NM_001166290.2:c.323_326delinsGCCT	NP_001159762.1:p.Arg108=
NM_001377296.1:c.323_326delinsGCCT	NP_001364225.1:p.Arg108=
NM_001377297.1:c.323_326delinsGCCT	NP_001364226.1:p.Arg108=
NM_000525.4:c.584_587delinsGCCT MANE Select	NP_000516.3:p.Arg195=