Canonical Allele Identifier: CA653978441

Gene: KCNJ11

Linked Data

• COSMIC: COSN22888181

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17386765_17386769del , CM000673.2:g.17386765_17386769del	GRCh38
NC_000011.9:g.17408312_17408316del , CM000673.1:g.17408312_17408316del	GRCh37
NC_000011.8:g.17364888_17364892del	NCBI36
NG_012446.1:g.6891_6895del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682350.1:c.*150_*154del	ENSP00000508090.1:n.*150_*154del
ENST00000682764.1:c.*50+100_*50+104del	ENSP00000506780.1:n.*50+100_*50+104del
ENST00000339994.5:c.*150_*154del MANE Select	ENSP00000345708.4:n.*150_*154del
ENST00000339994.4:c.*150_*154del	ENSP00000345708.4:n.*150_*154del
ENST00000528731.1:c.*150_*154del	ENSP00000434755.1:n.*150_*154del
NM_000525.3:c.*150_*154del	NP_000516.3:n.*150_*154del
NM_001166290.1:c.*150_*154del	NP_001159762.1:n.*150_*154del
XM_006718226.2:c.*150_*154del	XP_006718289.1:n.*150_*154del
XR_930867.1:n.1381+100_1381+104del
XM_006718226.3:c.*150_*154del	XP_006718289.1:n.*150_*154del
XM_017017680.1:c.*150_*154del	XP_016873169.1:n.*150_*154del
NM_001166290.2:c.*150_*154del	NP_001159762.1:n.*150_*154del
NM_001377296.1:c.*150_*154del	NP_001364225.1:n.*150_*154del
NM_001377297.1:c.*150_*154del	NP_001364226.1:n.*150_*154del
NM_000525.4:c.*150_*154del MANE Select	NP_000516.3:n.*150_*154del