Canonical Allele Identifier: CA1955118922

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17386743A= , CM000673.2:g.17386743A=	GRCh38
NC_000011.9:g.17408290A= , CM000673.1:g.17408290A=	GRCh37
NC_000011.8:g.17364866A=	NCBI36
NG_012446.1:g.6917T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000525.4:c.*176T= MANE Select	NP_000516.3:n.*176T=
ENST00000339994.5:c.*176T= MANE Select	ENSP00000345708.4:n.*176T=
NM_000525.3:c.*176T=	NP_000516.3:n.*176T=
NM_001166290.1:c.*176T=	NP_001159762.1:n.*176T=
NM_001166290.2:c.*176T=	NP_001159762.1:n.*176T=
NM_001377296.1:c.*176T=	NP_001364225.1:n.*176T=
NM_001377297.1:c.*176T=	NP_001364226.1:n.*176T=
ENST00000339994.4:c.*176T=	ENSP00000345708.4:n.*176T=
ENST00000526747.1:n.8T=
ENST00000528731.1:c.*176T=	ENSP00000434755.1:n.*176T=
ENST00000682350.1:c.*176T=	ENSP00000508090.1:n.*176T=
ENST00000682764.1:c.*50+126T=	ENSP00000506780.1:n.*50+126T=
XM_006718226.2:c.*176T=	XP_006718289.1:n.*176T=
XM_006718226.3:c.*176T=	XP_006718289.1:n.*176T=
XM_017017680.1:c.*176T=	XP_016873169.1:n.*176T=
XR_930867.1:n.1381+126T=