Canonical Allele Identifier: CA10607918

Gene: KCNJ10

Linked Data

• ClinVar Variation Id: 293113
• ClinVar RCV Id: RCV000334603 ; RCV000400580
• dbSNP Id: rs886045412
• gnomAD v3: 1-160041156-T-C
• gnomAD v4: 1-160041156-T-C
• MyVariant Identifiers: chr1:g.160010946T>C (hg19) ; chr1:g.160041156T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041156T>C , CM000663.2:g.160041156T>C	GRCh38
NC_000001.10:g.160010946T>C , CM000663.1:g.160010946T>C	GRCh37
NC_000001.9:g.158277570T>C	NCBI36
NG_016411.1:g.34016A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+678A>G
ENST00000636689.1:n.95-1808A>G
ENST00000637644.1:c.487+890A>G	ENSP00000490282.1:n.487+890A>G
ENST00000638728.1:c.*237A>G	ENSP00000492619.1:n.*237A>G
ENST00000638840.1:c.919+180A>G
ENST00000638868.1:c.*237A>G	ENSP00000491250.1:n.*237A>G
ENST00000639408.1:c.488-555A>G	ENSP00000491635.1:n.488-555A>G
ENST00000640017.1:c.670-555A>G	ENSP00000491337.1:n.670-555A>G
ENST00000640914.1:c.125-555A>G
ENST00000644903.1:c.*237A>G MANE Select	ENSP00000495557.1:n.*237A>G
ENST00000368089.3:c.*237A>G	ENSP00000357068.3:n.*237A>G
ENST00000509700.1:n.463-555A>G
NM_002241.4:c.*237A>G	NP_002232.2:n.*237A>G
NM_002241.5:c.*237A>G MANE Select	NP_002232.2:n.*237A>G