Canonical Allele Identifier: CA3003288155

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17386856_17386857insT , CM000673.2:g.17386856_17386857insT	GRCh38
NC_000011.9:g.17408403_17408404insT , CM000673.1:g.17408403_17408404insT	GRCh37
NC_000011.8:g.17364979_17364980insT	NCBI36
NG_012446.1:g.6803_6804insA

Transcript Alleles

HGVS	Amino-acid Change
NM_000525.4:c.*62_*63insA MANE Select	NP_000516.3:n.*62_*63insA
ENST00000339994.5:c.*62_*63insA MANE Select	ENSP00000345708.4:n.*62_*63insA
NM_000525.3:c.*62_*63insA	NP_000516.3:n.*62_*63insA
NM_001166290.1:c.*62_*63insA	NP_001159762.1:n.*62_*63insA
NM_001166290.2:c.*62_*63insA	NP_001159762.1:n.*62_*63insA
NM_001377296.1:c.*62_*63insA	NP_001364225.1:n.*62_*63insA
NM_001377297.1:c.*62_*63insA	NP_001364226.1:n.*62_*63insA
ENST00000339994.4:c.*62_*63insA	ENSP00000345708.4:n.*62_*63insA
ENST00000528731.1:c.*62_*63insA	ENSP00000434755.1:n.*62_*63insA
ENST00000682350.1:c.*62_*63insA	ENSP00000508090.1:n.*62_*63insA
ENST00000682764.1:c.*50+12_*50+13insA	ENSP00000506780.1:n.*50+12_*50+13insA
XM_006718226.2:c.*62_*63insA	XP_006718289.1:n.*62_*63insA
XM_006718226.3:c.*62_*63insA	XP_006718289.1:n.*62_*63insA
XM_017017680.1:c.*62_*63insA	XP_016873169.1:n.*62_*63insA
XR_930867.1:n.1381+12_1381+13insA