Canonical Allele Identifier: CA2840305411

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387223dup , CM000673.2:g.17387223dup	GRCh38
NC_000011.9:g.17408770dup , CM000673.1:g.17408770dup	GRCh37
NC_000011.8:g.17365346dup	NCBI36
NG_012446.1:g.6437dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682350.1:c.608dup	ENSP00000508090.1:p.Val204GlyfsTer18
ENST00000682764.1:c.608dup	ENSP00000506780.1:p.Val204GlyfsTer18
ENST00000339994.5:c.869dup MANE Select	ENSP00000345708.4:p.Val291GlyfsTer18
ENST00000339994.4:c.869dup	ENSP00000345708.4:p.Val291GlyfsTer18
ENST00000528731.1:c.608dup	ENSP00000434755.1:p.Val204GlyfsTer18
NM_000525.3:c.869dup	NP_000516.3:p.Val291GlyfsTer18
NM_001166290.1:c.608dup	NP_001159762.1:p.Val204GlyfsTer18
XM_006718226.2:c.608dup	XP_006718289.1:p.Val204GlyfsTer18
XR_930867.1:n.1027dup
XM_006718226.3:c.608dup	XP_006718289.1:p.Val204GlyfsTer18
XM_017017680.1:c.608dup	XP_016873169.1:p.Val204GlyfsTer18
NM_001166290.2:c.608dup	NP_001159762.1:p.Val204GlyfsTer18
NM_001377296.1:c.608dup	NP_001364225.1:p.Val204GlyfsTer18
NM_001377297.1:c.608dup	NP_001364226.1:p.Val204GlyfsTer18
NM_000525.4:c.869dup MANE Select	NP_000516.3:p.Val291GlyfsTer18