Canonical Allele Identifier: CA1955119478

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387994_17387995delinsGC , CM000673.2:g.17387994_17387995delinsGC	GRCh38
NC_000011.9:g.17409541_17409542delinsGC , CM000673.1:g.17409541_17409542delinsGC	GRCh37
NC_000011.8:g.17366117_17366118delinsGC	NCBI36
NG_012446.1:g.5665_5666delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.-132_-131delinsGC	ENSP00000436479.2:n.-132_-131delinsGC
ENST00000682350.1:c.-16-149_-16-148delinsGC	ENSP00000508090.1:n.-16-149_-16-148delinsGC
ENST00000682764.1:c.-16-149_-16-148delinsGC	ENSP00000506780.1:n.-16-149_-16-148delinsGC
ENST00000339994.5:c.97_98delinsGC MANE Select	ENSP00000345708.4:p.Ala33=
ENST00000339994.4:c.97_98delinsGC	ENSP00000345708.4:p.Ala33=
ENST00000526912.1:c.-17+23_-17+24delinsGC	ENSP00000432729.1:n.-17+23_-17+24delinsGC
ENST00000528731.1:c.-16-149_-16-148delinsGC	ENSP00000434755.1:n.-16-149_-16-148delinsGC
ENST00000528992.1:c.114_115delinsGC
NM_000525.3:c.97_98delinsGC	NP_000516.3:p.Ala33=
NM_001166290.1:c.-16-149_-16-148delinsGC	NP_001159762.1:n.-16-149_-16-148delinsGC
XM_006718226.2:c.-16-149_-16-148delinsGC	XP_006718289.1:n.-16-149_-16-148delinsGC
XR_930867.1:n.255_256delinsGC
XM_006718226.3:c.-16-149_-16-148delinsGC	XP_006718289.1:n.-16-149_-16-148delinsGC
XM_017017680.1:c.-16-149_-16-148delinsGC	XP_016873169.1:n.-16-149_-16-148delinsGC
NM_001166290.2:c.-16-149_-16-148delinsGC	NP_001159762.1:n.-16-149_-16-148delinsGC
NM_001377296.1:c.-17+23_-17+24delinsGC	NP_001364225.1:n.-17+23_-17+24delinsGC
NM_001377297.1:c.-16-149_-16-148delinsGC	NP_001364226.1:n.-16-149_-16-148delinsGC
NM_000525.4:c.97_98delinsGC MANE Select	NP_000516.3:p.Ala33=