Canonical Allele Identifier: CA5902294

Gene: KCNJ11

Linked Data

• ClinVar Variation Id: 1147260
• ClinVar RCV Id: RCV001486756
• dbSNP Id: rs752018515
• ExAC: 11:17409234 C / A
• gnomAD v2: 11-17409234-C-A
• gnomAD v3: 11-17387687-C-A
• gnomAD v4: 11-17387687-C-A
• MyVariant Identifiers: chr11:g.17409234C>A (hg19) ; chr11:g.17387687C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387687C>A , CM000673.2:g.17387687C>A	GRCh38
NC_000011.9:g.17409234C>A , CM000673.1:g.17409234C>A	GRCh37
NC_000011.8:g.17365810C>A	NCBI36
NG_012446.1:g.5973G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.177G>T	ENSP00000436479.2:p.Gly59=
ENST00000682350.1:c.144G>T	ENSP00000508090.1:p.Gly48=
ENST00000682764.1:c.144G>T	ENSP00000506780.1:p.Gly48=
ENST00000339994.5:c.405G>T MANE Select	ENSP00000345708.4:p.Gly135=
ENST00000339994.4:c.405G>T	ENSP00000345708.4:p.Gly135=
ENST00000526912.1:c.144G>T	ENSP00000432729.1:p.Gly48=
ENST00000528731.1:c.144G>T	ENSP00000434755.1:p.Gly48=
ENST00000528992.1:c.422G>T
NM_000525.3:c.405G>T	NP_000516.3:p.Gly135=
NM_001166290.1:c.144G>T	NP_001159762.1:p.Gly48=
XM_006718226.2:c.144G>T	XP_006718289.1:p.Gly48=
XR_930867.1:n.563G>T
XM_006718226.3:c.144G>T	XP_006718289.1:p.Gly48=
XM_017017680.1:c.144G>T	XP_016873169.1:p.Gly48=
NM_001166290.2:c.144G>T	NP_001159762.1:p.Gly48=
NM_001377296.1:c.144G>T	NP_001364225.1:p.Gly48=
NM_001377297.1:c.144G>T	NP_001364226.1:p.Gly48=
NM_000525.4:c.405G>T MANE Select	NP_000516.3:p.Gly135=