Canonical Allele Identifier: CA3184712949

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17386931A= , CM000673.2:g.17386931A=	GRCh38
NC_000011.9:g.17408478A= , CM000673.1:g.17408478A=	GRCh37
NC_000011.8:g.17365054A=	NCBI36
NG_012446.1:g.6729T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000525.4:c.1161T= MANE Select	NP_000516.3:p.Asp387=
ENST00000339994.5:c.1161T= MANE Select	ENSP00000345708.4:p.Asp387=
NM_000525.3:c.1161T=	NP_000516.3:p.Asp387=
NM_001166290.1:c.900T=	NP_001159762.1:p.Asp300=
NM_001166290.2:c.900T=	NP_001159762.1:p.Asp300=
NM_001377296.1:c.900T=	NP_001364225.1:p.Asp300=
NM_001377297.1:c.900T=	NP_001364226.1:p.Asp300=
ENST00000339994.4:c.1161T=	ENSP00000345708.4:p.Asp387=
ENST00000528731.1:c.900T=	ENSP00000434755.1:p.Asp300=
ENST00000682350.1:c.900T=	ENSP00000508090.1:p.Asp300=
ENST00000682764.1:c.900T=	ENSP00000506780.1:p.Asp300=
XM_006718226.2:c.900T=	XP_006718289.1:p.Asp300=
XM_006718226.3:c.900T=	XP_006718289.1:p.Asp300=
XM_017017680.1:c.900T=	XP_016873169.1:p.Asp300=
XR_930867.1:n.1319T=