Canonical Allele Identifier: CA1955119491

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17388025T= , CM000673.2:g.17388025T=	GRCh38
NC_000011.9:g.17409572T= , CM000673.1:g.17409572T=	GRCh37
NC_000011.8:g.17366148T=	NCBI36
NG_012446.1:g.5635A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000528992.2:c.-162A=	ENSP00000436479.2:n.-162A=
ENST00000682350.1:c.-16-179A=	ENSP00000508090.1:n.-16-179A=
ENST00000682764.1:c.-16-179A=	ENSP00000506780.1:n.-16-179A=
ENST00000339994.5:c.67A= MANE Select	ENSP00000345708.4:p.Lys23=
ENST00000339994.4:c.67A=	ENSP00000345708.4:p.Lys23=
ENST00000526912.1:c.-24A=	ENSP00000432729.1:n.-24A=
ENST00000528731.1:c.-16-179A=	ENSP00000434755.1:n.-16-179A=
ENST00000528992.1:c.84A=
NM_000525.3:c.67A=	NP_000516.3:p.Lys23=
NM_001166290.1:c.-16-179A=	NP_001159762.1:n.-16-179A=
XM_006718226.2:c.-16-179A=	XP_006718289.1:n.-16-179A=
XR_930867.1:n.225A=
XM_006718226.3:c.-16-179A=	XP_006718289.1:n.-16-179A=
XM_017017680.1:c.-16-179A=	XP_016873169.1:n.-16-179A=
NM_001166290.2:c.-16-179A=	NP_001159762.1:n.-16-179A=
NM_001377296.1:c.-24A=	NP_001364225.1:n.-24A=
NM_001377297.1:c.-16-179A=	NP_001364226.1:n.-16-179A=
NM_000525.4:c.67A= MANE Select	NP_000516.3:p.Lys23=