Canonical Allele Identifier: CA3003290126

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387929dup , CM000673.2:g.17387929dup	GRCh38
NC_000011.9:g.17409476dup , CM000673.1:g.17409476dup	GRCh37
NC_000011.8:g.17366052dup	NCBI36
NG_012446.1:g.5732dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.-65dup	ENSP00000436479.2:n.-65dup
ENST00000682350.1:c.-16-82dup	ENSP00000508090.1:n.-16-82dup
ENST00000682764.1:c.-16-82dup	ENSP00000506780.1:n.-16-82dup
ENST00000339994.5:c.164dup MANE Select	ENSP00000345708.4:p.Leu56ProfsTer?
ENST00000339994.4:c.164dup	ENSP00000345708.4:p.Leu56ProfsTer?
ENST00000526912.1:c.-16-82dup	ENSP00000432729.1:n.-16-82dup
ENST00000528731.1:c.-16-82dup	ENSP00000434755.1:n.-16-82dup
ENST00000528992.1:c.181dup
NM_000525.3:c.164dup	NP_000516.3:p.Leu56ProfsTer?
NM_001166290.1:c.-16-82dup	NP_001159762.1:n.-16-82dup
XM_006718226.2:c.-16-82dup	XP_006718289.1:n.-16-82dup
XR_930867.1:n.322dup
XM_006718226.3:c.-16-82dup	XP_006718289.1:n.-16-82dup
XM_017017680.1:c.-16-82dup	XP_016873169.1:n.-16-82dup
NM_001166290.2:c.-16-82dup	NP_001159762.1:n.-16-82dup
NM_001377296.1:c.-16-82dup	NP_001364225.1:n.-16-82dup
NM_001377297.1:c.-16-82dup	NP_001364226.1:n.-16-82dup
NM_000525.4:c.164dup MANE Select	NP_000516.3:p.Leu56ProfsTer?