Canonical Allele Identifier: CA5902160

Gene: KCNJ11

Linked Data

• dbSNP Id: rs765360093
• ExAC: 11:17408439 C / CT
• gnomAD v2: 11-17408439-C-CT
• gnomAD v4: 11-17386892-C-CT
• MyVariant Identifiers: chr11:g.17408439_17408440insT (hg19) ; chr11:g.17386892_17386893insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17386892_17386893insT , CM000673.2:g.17386892_17386893insT	GRCh38
NC_000011.9:g.17408439_17408440insT , CM000673.1:g.17408439_17408440insT	GRCh37
NC_000011.8:g.17365015_17365016insT	NCBI36
NG_012446.1:g.6767_6768insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682350.1:c.*26_*27insA	ENSP00000508090.1:n.*26_*27insA
ENST00000682764.1:c.*26_*27insA	ENSP00000506780.1:n.*26_*27insA
ENST00000339994.5:c.*26_*27insA MANE Select	ENSP00000345708.4:n.*26_*27insA
ENST00000339994.4:c.*26_*27insA	ENSP00000345708.4:n.*26_*27insA
ENST00000528731.1:c.*26_*27insA	ENSP00000434755.1:n.*26_*27insA
NM_000525.3:c.*26_*27insA	NP_000516.3:n.*26_*27insA
NM_001166290.1:c.*26_*27insA	NP_001159762.1:n.*26_*27insA
XM_006718226.2:c.*26_*27insA	XP_006718289.1:n.*26_*27insA
XR_930867.1:n.1357_1358insA
XM_006718226.3:c.*26_*27insA	XP_006718289.1:n.*26_*27insA
XM_017017680.1:c.*26_*27insA	XP_016873169.1:n.*26_*27insA
NM_001166290.2:c.*26_*27insA	NP_001159762.1:n.*26_*27insA
NM_001377296.1:c.*26_*27insA	NP_001364225.1:n.*26_*27insA
NM_001377297.1:c.*26_*27insA	NP_001364226.1:n.*26_*27insA
NM_000525.4:c.*26_*27insA MANE Select	NP_000516.3:n.*26_*27insA