Canonical Allele Identifier: CA1955119416

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387853_17387854delinsAG , CM000673.2:g.17387853_17387854delinsAG	GRCh38
NC_000011.9:g.17409400_17409401delinsAG , CM000673.1:g.17409400_17409401delinsAG	GRCh37
NC_000011.8:g.17365976_17365977delinsAG	NCBI36
NG_012446.1:g.5806_5807delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000528992.2:c.10_11delinsCT	ENSP00000436479.2:p.Leu4=
ENST00000682350.1:c.-16-8_-16-7delinsCT	ENSP00000508090.1:n.-16-8_-16-7delinsCT
ENST00000682764.1:c.-16-8_-16-7delinsCT	ENSP00000506780.1:n.-16-8_-16-7delinsCT
ENST00000339994.5:c.238_239delinsCT MANE Select	ENSP00000345708.4:p.Leu80=
ENST00000339994.4:c.238_239delinsCT	ENSP00000345708.4:p.Leu80=
ENST00000526912.1:c.-16-8_-16-7delinsCT	ENSP00000432729.1:n.-16-8_-16-7delinsCT
ENST00000528731.1:c.-16-8_-16-7delinsCT	ENSP00000434755.1:n.-16-8_-16-7delinsCT
ENST00000528992.1:c.255_256delinsCT
NM_000525.3:c.238_239delinsCT	NP_000516.3:p.Leu80=
NM_001166290.1:c.-16-8_-16-7delinsCT	NP_001159762.1:n.-16-8_-16-7delinsCT
XM_006718226.2:c.-16-8_-16-7delinsCT	XP_006718289.1:n.-16-8_-16-7delinsCT
XR_930867.1:n.396_397delinsCT
XM_006718226.3:c.-16-8_-16-7delinsCT	XP_006718289.1:n.-16-8_-16-7delinsCT
XM_017017680.1:c.-16-8_-16-7delinsCT	XP_016873169.1:n.-16-8_-16-7delinsCT
NM_001166290.2:c.-16-8_-16-7delinsCT	NP_001159762.1:n.-16-8_-16-7delinsCT
NM_001377296.1:c.-16-8_-16-7delinsCT	NP_001364225.1:n.-16-8_-16-7delinsCT
NM_001377297.1:c.-16-8_-16-7delinsCT	NP_001364226.1:n.-16-8_-16-7delinsCT
NM_000525.4:c.238_239delinsCT MANE Select	NP_000516.3:p.Leu80=