Canonical Allele Identifier: CA1955119609

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17388233A= , CM000673.2:g.17388233A=	GRCh38
NC_000011.9:g.17409780A= , CM000673.1:g.17409780A=	GRCh37
NC_000011.8:g.17366356A=	NCBI36
NG_012446.1:g.5427T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000528992.2:c.-213-157T=	ENSP00000436479.2:n.-213-157T=
ENST00000682350.1:c.-16-387T=	ENSP00000508090.1:n.-16-387T=
ENST00000682764.1:c.-16-387T=	ENSP00000506780.1:n.-16-387T=
ENST00000339994.5:c.-142T= MANE Select	ENSP00000345708.4:n.-142T=
ENST00000339994.4:c.-142T=	ENSP00000345708.4:n.-142T=
ENST00000526912.1:c.-75-157T=	ENSP00000432729.1:n.-75-157T=
ENST00000528731.1:c.-16-387T=	ENSP00000434755.1:n.-16-387T=
ENST00000528992.1:c.33-157T=
NM_000525.3:c.-142T=	NP_000516.3:n.-142T=
NM_001166290.1:c.-16-387T=	NP_001159762.1:n.-16-387T=
XM_006718226.2:c.-16-387T=	XP_006718289.1:n.-16-387T=
XR_930867.1:n.17T=
XM_006718226.3:c.-16-387T=	XP_006718289.1:n.-16-387T=
XM_017017680.1:c.-16-387T=	XP_016873169.1:n.-16-387T=
NM_001166290.2:c.-16-387T=	NP_001159762.1:n.-16-387T=
NM_001377296.1:c.-75-157T=	NP_001364225.1:n.-75-157T=
NM_001377297.1:c.-16-387T=	NP_001364226.1:n.-16-387T=
NM_000525.4:c.-142T= MANE Select	NP_000516.3:n.-142T=