Canonical Allele Identifier: CA2612640408

Gene: KCNJ11

Linked Data

• gnomAD v4: 11-17388220-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17388220_17388221insA , CM000673.2:g.17388220_17388221insA	GRCh38
NC_000011.9:g.17409767_17409768insA , CM000673.1:g.17409767_17409768insA	GRCh37
NC_000011.8:g.17366343_17366344insA	NCBI36
NG_012446.1:g.5439_5440insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.-213-145_-213-144insT	ENSP00000436479.2:n.-213-145_-213-144insT
ENST00000682350.1:c.-16-375_-16-374insT	ENSP00000508090.1:n.-16-375_-16-374insT
ENST00000682764.1:c.-16-375_-16-374insT	ENSP00000506780.1:n.-16-375_-16-374insT
ENST00000339994.5:c.-130_-129insT MANE Select	ENSP00000345708.4:n.-130_-129insT
ENST00000339994.4:c.-130_-129insT	ENSP00000345708.4:n.-130_-129insT
ENST00000526912.1:c.-75-145_-75-144insT	ENSP00000432729.1:n.-75-145_-75-144insT
ENST00000528731.1:c.-16-375_-16-374insT	ENSP00000434755.1:n.-16-375_-16-374insT
ENST00000528992.1:c.33-145_33-144insT
NM_000525.3:c.-130_-129insT	NP_000516.3:n.-130_-129insT
NM_001166290.1:c.-16-375_-16-374insT	NP_001159762.1:n.-16-375_-16-374insT
XM_006718226.2:c.-16-375_-16-374insT	XP_006718289.1:n.-16-375_-16-374insT
XR_930867.1:n.29_30insT
XM_006718226.3:c.-16-375_-16-374insT	XP_006718289.1:n.-16-375_-16-374insT
XM_017017680.1:c.-16-375_-16-374insT	XP_016873169.1:n.-16-375_-16-374insT
NM_001166290.2:c.-16-375_-16-374insT	NP_001159762.1:n.-16-375_-16-374insT
NM_001377296.1:c.-75-145_-75-144insT	NP_001364225.1:n.-75-145_-75-144insT
NM_001377297.1:c.-16-375_-16-374insT	NP_001364226.1:n.-16-375_-16-374insT
NM_000525.4:c.-130_-129insT MANE Select	NP_000516.3:n.-130_-129insT