Canonical Allele Identifier: CA935521361

Gene: KCNJ11

Linked Data

• dbSNP Id: rs1953565934
• gnomAD v3: 11-17386896-T-TG
• gnomAD v4: 11-17386896-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17386902dup , CM000673.2:g.17386902dup	GRCh38
NC_000011.9:g.17408449dup , CM000673.1:g.17408449dup	GRCh37
NC_000011.8:g.17365025dup	NCBI36
NG_012446.1:g.6763dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682350.1:c.*22dup	ENSP00000508090.1:n.*22dup
ENST00000682764.1:c.*22dup	ENSP00000506780.1:n.*22dup
ENST00000339994.5:c.*22dup MANE Select	ENSP00000345708.4:n.*22dup
ENST00000339994.4:c.*22dup	ENSP00000345708.4:n.*22dup
ENST00000528731.1:c.*22dup	ENSP00000434755.1:n.*22dup
NM_000525.3:c.*22dup	NP_000516.3:n.*22dup
NM_001166290.1:c.*22dup	NP_001159762.1:n.*22dup
XM_006718226.2:c.*22dup	XP_006718289.1:n.*22dup
XR_930867.1:n.1353dup
XM_006718226.3:c.*22dup	XP_006718289.1:n.*22dup
XM_017017680.1:c.*22dup	XP_016873169.1:n.*22dup
NM_001166290.2:c.*22dup	NP_001159762.1:n.*22dup
NM_001377296.1:c.*22dup	NP_001364225.1:n.*22dup
NM_001377297.1:c.*22dup	NP_001364226.1:n.*22dup
NM_000525.4:c.*22dup MANE Select	NP_000516.3:n.*22dup