Canonical Allele Identifier: CA1955119070

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17386989_17386990delinsAG , CM000673.2:g.17386989_17386990delinsAG	GRCh38
NC_000011.9:g.17408536_17408537delinsAG , CM000673.1:g.17408536_17408537delinsAG	GRCh37
NC_000011.8:g.17365112_17365113delinsAG	NCBI36
NG_012446.1:g.6670_6671delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000682350.1:c.841_842delinsCT	ENSP00000508090.1:p.Leu281=
ENST00000682764.1:c.841_842delinsCT	ENSP00000506780.1:p.Leu281=
ENST00000339994.5:c.1102_1103delinsCT MANE Select	ENSP00000345708.4:p.Leu368=
ENST00000339994.4:c.1102_1103delinsCT	ENSP00000345708.4:p.Leu368=
ENST00000528731.1:c.841_842delinsCT	ENSP00000434755.1:p.Leu281=
NM_000525.3:c.1102_1103delinsCT	NP_000516.3:p.Leu368=
NM_001166290.1:c.841_842delinsCT	NP_001159762.1:p.Leu281=
XM_006718226.2:c.841_842delinsCT	XP_006718289.1:p.Leu281=
XR_930867.1:n.1260_1261delinsCT
XM_006718226.3:c.841_842delinsCT	XP_006718289.1:p.Leu281=
XM_017017680.1:c.841_842delinsCT	XP_016873169.1:p.Leu281=
NM_001166290.2:c.841_842delinsCT	NP_001159762.1:p.Leu281=
NM_001377296.1:c.841_842delinsCT	NP_001364225.1:p.Leu281=
NM_001377297.1:c.841_842delinsCT	NP_001364226.1:p.Leu281=
NM_000525.4:c.1102_1103delinsCT MANE Select	NP_000516.3:p.Leu368=