Canonical Allele Identifier: CA1955119369

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387733_17387734delinsGC , CM000673.2:g.17387733_17387734delinsGC	GRCh38
NC_000011.9:g.17409280_17409281delinsGC , CM000673.1:g.17409280_17409281delinsGC	GRCh37
NC_000011.8:g.17365856_17365857delinsGC	NCBI36
NG_012446.1:g.5926_5927delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.130_131delinsGC	ENSP00000436479.2:p.Ala44=
ENST00000682350.1:c.97_98delinsGC	ENSP00000508090.1:p.Ala33=
ENST00000682764.1:c.97_98delinsGC	ENSP00000506780.1:p.Ala33=
ENST00000339994.5:c.358_359delinsGC MANE Select	ENSP00000345708.4:p.Ala120=
ENST00000339994.4:c.358_359delinsGC	ENSP00000345708.4:p.Ala120=
ENST00000526912.1:c.97_98delinsGC	ENSP00000432729.1:p.Ala33=
ENST00000528731.1:c.97_98delinsGC	ENSP00000434755.1:p.Ala33=
ENST00000528992.1:c.375_376delinsGC
NM_000525.3:c.358_359delinsGC	NP_000516.3:p.Ala120=
NM_001166290.1:c.97_98delinsGC	NP_001159762.1:p.Ala33=
XM_006718226.2:c.97_98delinsGC	XP_006718289.1:p.Ala33=
XR_930867.1:n.516_517delinsGC
XM_006718226.3:c.97_98delinsGC	XP_006718289.1:p.Ala33=
XM_017017680.1:c.97_98delinsGC	XP_016873169.1:p.Ala33=
NM_001166290.2:c.97_98delinsGC	NP_001159762.1:p.Ala33=
NM_001377296.1:c.97_98delinsGC	NP_001364225.1:p.Ala33=
NM_001377297.1:c.97_98delinsGC	NP_001364226.1:p.Ala33=
NM_000525.4:c.358_359delinsGC MANE Select	NP_000516.3:p.Ala120=