Canonical Allele Identifier: CA1955119519

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17388075C= , CM000673.2:g.17388075C=	GRCh38
NC_000011.9:g.17409622C= , CM000673.1:g.17409622C=	GRCh37
NC_000011.8:g.17366198C=	NCBI36
NG_012446.1:g.5585G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.-212G=	ENSP00000436479.2:n.-212G=
ENST00000682350.1:c.-16-229G=	ENSP00000508090.1:n.-16-229G=
ENST00000682764.1:c.-16-229G=	ENSP00000506780.1:n.-16-229G=
ENST00000339994.5:c.17G= MANE Select	ENSP00000345708.4:p.Gly6=
ENST00000339994.4:c.17G=	ENSP00000345708.4:p.Gly6=
ENST00000526912.1:c.-74G=	ENSP00000432729.1:n.-74G=
ENST00000528731.1:c.-16-229G=	ENSP00000434755.1:n.-16-229G=
ENST00000528992.1:c.34G=
NM_000525.3:c.17G=	NP_000516.3:p.Gly6=
NM_001166290.1:c.-16-229G=	NP_001159762.1:n.-16-229G=
XM_006718226.2:c.-16-229G=	XP_006718289.1:n.-16-229G=
XR_930867.1:n.175G=
XM_006718226.3:c.-16-229G=	XP_006718289.1:n.-16-229G=
XM_017017680.1:c.-16-229G=	XP_016873169.1:n.-16-229G=
NM_001166290.2:c.-16-229G=	NP_001159762.1:n.-16-229G=
NM_001377296.1:c.-74G=	NP_001364225.1:n.-74G=
NM_001377297.1:c.-16-229G=	NP_001364226.1:n.-16-229G=
NM_000525.4:c.17G= MANE Select	NP_000516.3:p.Gly6=