Canonical Allele Identifier: CA1955119634

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17388274_17388275delinsCA , CM000673.2:g.17388274_17388275delinsCA	GRCh38
NC_000011.9:g.17409821_17409822delinsCA , CM000673.1:g.17409821_17409822delinsCA	GRCh37
NC_000011.8:g.17366397_17366398delinsCA	NCBI36
NG_012446.1:g.5385_5386delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.-213-199_-213-198delinsTG	ENSP00000436479.2:n.-213-199_-213-198delinsTG
ENST00000682350.1:c.-16-429_-16-428delinsTG	ENSP00000508090.1:n.-16-429_-16-428delinsTG
ENST00000682764.1:c.-16-429_-16-428delinsTG	ENSP00000506780.1:n.-16-429_-16-428delinsTG
ENST00000339994.5:c.-184_-183delinsTG MANE Select	ENSP00000345708.4:n.-184_-183delinsTG
ENST00000339994.4:c.-184_-183delinsTG	ENSP00000345708.4:n.-184_-183delinsTG
ENST00000526912.1:c.-75-199_-75-198delinsTG	ENSP00000432729.1:n.-75-199_-75-198delinsTG
ENST00000528731.1:c.-16-429_-16-428delinsTG	ENSP00000434755.1:n.-16-429_-16-428delinsTG
ENST00000528992.1:c.33-199_33-198delinsTG
NM_000525.3:c.-184_-183delinsTG	NP_000516.3:n.-184_-183delinsTG
NM_001166290.1:c.-16-429_-16-428delinsTG	NP_001159762.1:n.-16-429_-16-428delinsTG
XM_006718226.2:c.-16-429_-16-428delinsTG	XP_006718289.1:n.-16-429_-16-428delinsTG
XM_006718226.3:c.-16-429_-16-428delinsTG	XP_006718289.1:n.-16-429_-16-428delinsTG
XM_017017680.1:c.-16-429_-16-428delinsTG	XP_016873169.1:n.-16-429_-16-428delinsTG
NM_001166290.2:c.-16-429_-16-428delinsTG	NP_001159762.1:n.-16-429_-16-428delinsTG
NM_001377296.1:c.-75-199_-75-198delinsTG	NP_001364225.1:n.-75-199_-75-198delinsTG
NM_001377297.1:c.-16-429_-16-428delinsTG	NP_001364226.1:n.-16-429_-16-428delinsTG
NM_000525.4:c.-184_-183delinsTG MANE Select	NP_000516.3:n.-184_-183delinsTG