Canonical Allele Identifier: CA1955119574

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17388174T= , CM000673.2:g.17388174T=	GRCh38
NC_000011.9:g.17409721T= , CM000673.1:g.17409721T=	GRCh37
NC_000011.8:g.17366297T=	NCBI36
NG_012446.1:g.5486A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.-213-98A=	ENSP00000436479.2:n.-213-98A=
ENST00000682350.1:c.-16-328A=	ENSP00000508090.1:n.-16-328A=
ENST00000682764.1:c.-16-328A=	ENSP00000506780.1:n.-16-328A=
ENST00000339994.5:c.-83A= MANE Select	ENSP00000345708.4:n.-83A=
ENST00000339994.4:c.-83A=	ENSP00000345708.4:n.-83A=
ENST00000526912.1:c.-75-98A=	ENSP00000432729.1:n.-75-98A=
ENST00000528731.1:c.-16-328A=	ENSP00000434755.1:n.-16-328A=
ENST00000528992.1:c.33-98A=
NM_000525.3:c.-83A=	NP_000516.3:n.-83A=
NM_001166290.1:c.-16-328A=	NP_001159762.1:n.-16-328A=
XM_006718226.2:c.-16-328A=	XP_006718289.1:n.-16-328A=
XR_930867.1:n.76A=
XM_006718226.3:c.-16-328A=	XP_006718289.1:n.-16-328A=
XM_017017680.1:c.-16-328A=	XP_016873169.1:n.-16-328A=
NM_001166290.2:c.-16-328A=	NP_001159762.1:n.-16-328A=
NM_001377296.1:c.-75-98A=	NP_001364225.1:n.-75-98A=
NM_001377297.1:c.-16-328A=	NP_001364226.1:n.-16-328A=
NM_000525.4:c.-83A= MANE Select	NP_000516.3:n.-83A=