Canonical Allele Identifier: CA3003290462

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17388030_17388031insA , CM000673.2:g.17388030_17388031insA	GRCh38
NC_000011.9:g.17409577_17409578insA , CM000673.1:g.17409577_17409578insA	GRCh37
NC_000011.8:g.17366153_17366154insA	NCBI36
NG_012446.1:g.5629_5630insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.-168_-167insT	ENSP00000436479.2:n.-168_-167insT
ENST00000682350.1:c.-16-185_-16-184insT	ENSP00000508090.1:n.-16-185_-16-184insT
ENST00000682764.1:c.-16-185_-16-184insT	ENSP00000506780.1:n.-16-185_-16-184insT
ENST00000339994.5:c.61_62insT MANE Select	ENSP00000345708.4:p.Pro21LeufsTer?
ENST00000339994.4:c.61_62insT	ENSP00000345708.4:p.Pro21LeufsTer?
ENST00000526912.1:c.-30_-29insT	ENSP00000432729.1:n.-30_-29insT
ENST00000528731.1:c.-16-185_-16-184insT	ENSP00000434755.1:n.-16-185_-16-184insT
ENST00000528992.1:c.78_79insT
NM_000525.3:c.61_62insT	NP_000516.3:p.Pro21LeufsTer?
NM_001166290.1:c.-16-185_-16-184insT	NP_001159762.1:n.-16-185_-16-184insT
XM_006718226.2:c.-16-185_-16-184insT	XP_006718289.1:n.-16-185_-16-184insT
XR_930867.1:n.219_220insT
XM_006718226.3:c.-16-185_-16-184insT	XP_006718289.1:n.-16-185_-16-184insT
XM_017017680.1:c.-16-185_-16-184insT	XP_016873169.1:n.-16-185_-16-184insT
NM_001166290.2:c.-16-185_-16-184insT	NP_001159762.1:n.-16-185_-16-184insT
NM_001377296.1:c.-30_-29insT	NP_001364225.1:n.-30_-29insT
NM_001377297.1:c.-16-185_-16-184insT	NP_001364226.1:n.-16-185_-16-184insT
NM_000525.4:c.61_62insT MANE Select	NP_000516.3:p.Pro21LeufsTer?