Canonical Allele Identifier: CA1955119405

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387813G= , CM000673.2:g.17387813G=	GRCh38
NC_000011.9:g.17409360G= , CM000673.1:g.17409360G=	GRCh37
NC_000011.8:g.17365936G=	NCBI36
NG_012446.1:g.5847C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000528992.2:c.51C=	ENSP00000436479.2:p.Ile17=
ENST00000682350.1:c.18C=	ENSP00000508090.1:p.Ile6=
ENST00000682764.1:c.18C=	ENSP00000506780.1:p.Ile6=
ENST00000339994.5:c.279C= MANE Select	ENSP00000345708.4:p.Ile93=
ENST00000339994.4:c.279C=	ENSP00000345708.4:p.Ile93=
ENST00000526912.1:c.18C=	ENSP00000432729.1:p.Ile6=
ENST00000528731.1:c.18C=	ENSP00000434755.1:p.Ile6=
ENST00000528992.1:c.296C=
NM_000525.3:c.279C=	NP_000516.3:p.Ile93=
NM_001166290.1:c.18C=	NP_001159762.1:p.Ile6=
XM_006718226.2:c.18C=	XP_006718289.1:p.Ile6=
XR_930867.1:n.437C=
XM_006718226.3:c.18C=	XP_006718289.1:p.Ile6=
XM_017017680.1:c.18C=	XP_016873169.1:p.Ile6=
NM_001166290.2:c.18C=	NP_001159762.1:p.Ile6=
NM_001377296.1:c.18C=	NP_001364225.1:p.Ile6=
NM_001377297.1:c.18C=	NP_001364226.1:p.Ile6=
NM_000525.4:c.279C= MANE Select	NP_000516.3:p.Ile93=