Canonical Allele Identifier: CA3189256524

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17386859G= , CM000673.2:g.17386859G=	GRCh38
NC_000011.9:g.17408406G= , CM000673.1:g.17408406G=	GRCh37
NC_000011.8:g.17364982G=	NCBI36
NG_012446.1:g.6801C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000525.4:c.*60C= MANE Select	NP_000516.3:n.*60C=
ENST00000339994.5:c.*60C= MANE Select	ENSP00000345708.4:n.*60C=
NM_000525.3:c.*60C=	NP_000516.3:n.*60C=
NM_001166290.1:c.*60C=	NP_001159762.1:n.*60C=
NM_001166290.2:c.*60C=	NP_001159762.1:n.*60C=
NM_001377296.1:c.*60C=	NP_001364225.1:n.*60C=
NM_001377297.1:c.*60C=	NP_001364226.1:n.*60C=
ENST00000339994.4:c.*60C=	ENSP00000345708.4:n.*60C=
ENST00000528731.1:c.*60C=	ENSP00000434755.1:n.*60C=
ENST00000682350.1:c.*60C=	ENSP00000508090.1:n.*60C=
ENST00000682764.1:c.*50+10C=	ENSP00000506780.1:n.*50+10C=
XM_006718226.2:c.*60C=	XP_006718289.1:n.*60C=
XM_006718226.3:c.*60C=	XP_006718289.1:n.*60C=
XM_017017680.1:c.*60C=	XP_016873169.1:n.*60C=
XR_930867.1:n.1381+10C=