Canonical Allele Identifier: CA1955119494

Gene: KCNJ11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17388029_17388030delinsAG , CM000673.2:g.17388029_17388030delinsAG	GRCh38
NC_000011.9:g.17409576_17409577delinsAG , CM000673.1:g.17409576_17409577delinsAG	GRCh37
NC_000011.8:g.17366152_17366153delinsAG	NCBI36
NG_012446.1:g.5630_5631delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000528992.2:c.-167_-166delinsCT	ENSP00000436479.2:n.-167_-166delinsCT
ENST00000682350.1:c.-16-184_-16-183delinsCT	ENSP00000508090.1:n.-16-184_-16-183delins...
ENST00000682764.1:c.-16-184_-16-183delinsCT	ENSP00000506780.1:n.-16-184_-16-183delins...
ENST00000339994.5:c.62_63delinsCT MANE Select	ENSP00000345708.4:p.Pro21=
ENST00000339994.4:c.62_63delinsCT	ENSP00000345708.4:p.Pro21=
ENST00000526912.1:c.-29_-28delinsCT	ENSP00000432729.1:n.-29_-28delinsCT
ENST00000528731.1:c.-16-184_-16-183delinsCT	ENSP00000434755.1:n.-16-184_-16-183delins...
ENST00000528992.1:c.79_80delinsCT
NM_000525.3:c.62_63delinsCT	NP_000516.3:p.Pro21=
NM_001166290.1:c.-16-184_-16-183delinsCT	NP_001159762.1:n.-16-184_-16-183delinsCT
XM_006718226.2:c.-16-184_-16-183delinsCT	XP_006718289.1:n.-16-184_-16-183delinsCT
XR_930867.1:n.220_221delinsCT
XM_006718226.3:c.-16-184_-16-183delinsCT	XP_006718289.1:n.-16-184_-16-183delinsCT
XM_017017680.1:c.-16-184_-16-183delinsCT	XP_016873169.1:n.-16-184_-16-183delinsCT
NM_001166290.2:c.-16-184_-16-183delinsCT	NP_001159762.1:n.-16-184_-16-183delinsCT
NM_001377296.1:c.-29_-28delinsCT	NP_001364225.1:n.-29_-28delinsCT
NM_001377297.1:c.-16-184_-16-183delinsCT	NP_001364226.1:n.-16-184_-16-183delinsCT
NM_000525.4:c.62_63delinsCT MANE Select	NP_000516.3:p.Pro21=