Canonical Allele Identifier: CA1955119099

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387048C= , CM000673.2:g.17387048C=	GRCh38
NC_000011.9:g.17408595C= , CM000673.1:g.17408595C=	GRCh37
NC_000011.8:g.17365171C=	NCBI36
NG_012446.1:g.6612G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682350.1:c.783G=	ENSP00000508090.1:p.Gln261=
ENST00000682764.1:c.783G=	ENSP00000506780.1:p.Gln261=
ENST00000339994.5:c.1044G= MANE Select	ENSP00000345708.4:p.Gln348=
ENST00000339994.4:c.1044G=	ENSP00000345708.4:p.Gln348=
ENST00000528731.1:c.783G=	ENSP00000434755.1:p.Gln261=
NM_000525.3:c.1044G=	NP_000516.3:p.Gln348=
NM_001166290.1:c.783G=	NP_001159762.1:p.Gln261=
XM_006718226.2:c.783G=	XP_006718289.1:p.Gln261=
XR_930867.1:n.1202G=
XM_006718226.3:c.783G=	XP_006718289.1:p.Gln261=
XM_017017680.1:c.783G=	XP_016873169.1:p.Gln261=
NM_001166290.2:c.783G=	NP_001159762.1:p.Gln261=
NM_001377296.1:c.783G=	NP_001364225.1:p.Gln261=
NM_001377297.1:c.783G=	NP_001364226.1:p.Gln261=
NM_000525.4:c.1044G= MANE Select	NP_000516.3:p.Gln348=