Canonical Allele Identifier: CA2525269193

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17388197_17388202del , CM000673.2:g.17388197_17388202del	GRCh38
NC_000011.9:g.17409744_17409749del , CM000673.1:g.17409744_17409749del	GRCh37
NC_000011.8:g.17366320_17366325del	NCBI36
NG_012446.1:g.5461_5466del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.-213-123_-213-118del	ENSP00000436479.2:n.-213-123_-213-118del
ENST00000682350.1:c.-16-353_-16-348del	ENSP00000508090.1:n.-16-353_-16-348del
ENST00000682764.1:c.-16-353_-16-348del	ENSP00000506780.1:n.-16-353_-16-348del
ENST00000339994.5:c.-108_-103del MANE Select	ENSP00000345708.4:n.-108_-103del
ENST00000339994.4:c.-108_-103del	ENSP00000345708.4:n.-108_-103del
ENST00000526912.1:c.-75-123_-75-118del	ENSP00000432729.1:n.-75-123_-75-118del
ENST00000528731.1:c.-16-353_-16-348del	ENSP00000434755.1:n.-16-353_-16-348del
ENST00000528992.1:c.33-123_33-118del
NM_000525.3:c.-108_-103del	NP_000516.3:n.-108_-103del
NM_001166290.1:c.-16-353_-16-348del	NP_001159762.1:n.-16-353_-16-348del
XM_006718226.2:c.-16-353_-16-348del	XP_006718289.1:n.-16-353_-16-348del
XR_930867.1:n.51_56del
XM_006718226.3:c.-16-353_-16-348del	XP_006718289.1:n.-16-353_-16-348del
XM_017017680.1:c.-16-353_-16-348del	XP_016873169.1:n.-16-353_-16-348del
NM_001166290.2:c.-16-353_-16-348del	NP_001159762.1:n.-16-353_-16-348del
NM_001377296.1:c.-75-123_-75-118del	NP_001364225.1:n.-75-123_-75-118del
NM_001377297.1:c.-16-353_-16-348del	NP_001364226.1:n.-16-353_-16-348del
NM_000525.4:c.-108_-103del MANE Select	NP_000516.3:n.-108_-103del