Canonical Allele Identifier: CA473515637

Gene: KCNJ11

Linked Data

• ClinVar Variation Id: 1136523
• ClinVar RCV Id: RCV001472188
• dbSNP Id: rs1351801133
• gnomAD v2: 11-17409282-A-C
• gnomAD v3: 11-17387735-A-C
• gnomAD v4: 11-17387735-A-C
• MyVariant Identifiers: chr11:g.17409282A>C (hg19) ; chr11:g.17387735A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387735A>C , CM000673.2:g.17387735A>C	GRCh38
NC_000011.9:g.17409282A>C , CM000673.1:g.17409282A>C	GRCh37
NC_000011.8:g.17365858A>C	NCBI36
NG_012446.1:g.5925T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528992.2:c.129T>G	ENSP00000436479.2:p.Ser43=
ENST00000682350.1:c.96T>G	ENSP00000508090.1:p.Ser32=
ENST00000682764.1:c.96T>G	ENSP00000506780.1:p.Ser32=
ENST00000339994.5:c.357T>G MANE Select	ENSP00000345708.4:p.Ser119=
ENST00000339994.4:c.357T>G	ENSP00000345708.4:p.Ser119=
ENST00000526912.1:c.96T>G	ENSP00000432729.1:p.Ser32=
ENST00000528731.1:c.96T>G	ENSP00000434755.1:p.Ser32=
ENST00000528992.1:c.374T>G
NM_000525.3:c.357T>G	NP_000516.3:p.Ser119=
NM_001166290.1:c.96T>G	NP_001159762.1:p.Ser32=
XM_006718226.2:c.96T>G	XP_006718289.1:p.Ser32=
XR_930867.1:n.515T>G
XM_006718226.3:c.96T>G	XP_006718289.1:p.Ser32=
XM_017017680.1:c.96T>G	XP_016873169.1:p.Ser32=
NM_001166290.2:c.96T>G	NP_001159762.1:p.Ser32=
NM_001377296.1:c.96T>G	NP_001364225.1:p.Ser32=
NM_001377297.1:c.96T>G	NP_001364226.1:p.Ser32=
NM_000525.4:c.357T>G MANE Select	NP_000516.3:p.Ser119=