Canonical Allele Identifier: CA3189255872

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17386761C= , CM000673.2:g.17386761C=	GRCh38
NC_000011.9:g.17408308C= , CM000673.1:g.17408308C=	GRCh37
NC_000011.8:g.17364884C=	NCBI36
NG_012446.1:g.6899G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000525.4:c.*158G= MANE Select	NP_000516.3:n.*158G=
ENST00000339994.5:c.*158G= MANE Select	ENSP00000345708.4:n.*158G=
NM_000525.3:c.*158G=	NP_000516.3:n.*158G=
NM_001166290.1:c.*158G=	NP_001159762.1:n.*158G=
NM_001166290.2:c.*158G=	NP_001159762.1:n.*158G=
NM_001377296.1:c.*158G=	NP_001364225.1:n.*158G=
NM_001377297.1:c.*158G=	NP_001364226.1:n.*158G=
ENST00000339994.4:c.*158G=	ENSP00000345708.4:n.*158G=
ENST00000528731.1:c.*158G=	ENSP00000434755.1:n.*158G=
ENST00000682350.1:c.*158G=	ENSP00000508090.1:n.*158G=
ENST00000682764.1:c.*50+108G=	ENSP00000506780.1:n.*50+108G=
XM_006718226.2:c.*158G=	XP_006718289.1:n.*158G=
XM_006718226.3:c.*158G=	XP_006718289.1:n.*158G=
XM_017017680.1:c.*158G=	XP_016873169.1:n.*158G=
XR_930867.1:n.1381+108G=