Canonical Allele Identifier: CA31469764

Gene: KCNJ10

Linked Data

• ClinVar Variation Id: 1191627
• ClinVar RCV Id: RCV001552777
• dbSNP Id: rs115725914
• gnomAD v2: 1-160011046-C-T
• gnomAD v3: 1-160041256-C-T
• gnomAD v4: 1-160041256-C-T
• MyVariant Identifiers: chr1:g.160011046C>T (hg19) ; chr1:g.160041256C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041256C>T , CM000663.2:g.160041256C>T	GRCh38
NC_000001.10:g.160011046C>T , CM000663.1:g.160011046C>T	GRCh37
NC_000001.9:g.158277670C>T	NCBI36
NG_016411.1:g.33916G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+578G>A
ENST00000636689.1:n.95-1908G>A
ENST00000637644.1:c.487+790G>A	ENSP00000490282.1:n.487+790G>A
ENST00000638728.1:c.*137G>A	ENSP00000492619.1:n.*137G>A
ENST00000638840.1:c.919+80G>A
ENST00000638868.1:c.*137G>A	ENSP00000491250.1:n.*137G>A
ENST00000639408.1:c.488-655G>A	ENSP00000491635.1:n.488-655G>A
ENST00000640017.1:c.669+578G>A	ENSP00000491337.1:n.669+578G>A
ENST00000640914.1:c.124+578G>A
ENST00000644903.1:c.*137G>A MANE Select	ENSP00000495557.1:n.*137G>A
ENST00000368089.3:c.*137G>A	ENSP00000357068.3:n.*137G>A
ENST00000509700.1:n.462+578G>A
NM_002241.4:c.*137G>A	NP_002232.2:n.*137G>A
NM_002241.5:c.*137G>A MANE Select	NP_002232.2:n.*137G>A