Canonical Allele Identifier: CA343222508
Gene: KCNJ10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1163174
ClinVar RCV Id: RCV001508013
dbSNP Id: rs2101924603

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160041502T>C , CM000663.2:g.160041502T>C GRCh38
NC_000001.10:g.160011292T>C , CM000663.1:g.160011292T>C GRCh37
NC_000001.9:g.158277916T>C NCBI36
NG_016411.1:g.33670A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.671+332A>G
ENST00000636689.1:n.95-2154A>G
ENST00000637644.1:c.487+544A>G ENSP00000490282.1:n.487+544A>G
ENST00000638728.1:c.1031A>G ENSP00000492619.1:p.Asp344Gly
ENST00000638840.1:c.753A>G
ENST00000638868.1:c.1031A>G ENSP00000491250.1:p.Asp344Gly
ENST00000639408.1:c.487+544A>G ENSP00000491635.1:n.487+544A>G
ENST00000640017.1:c.669+332A>G ENSP00000491337.1:n.669+332A>G
ENST00000640914.1:c.124+332A>G
ENST00000644903.1:c.1031A>G MANE Select ENSP00000495557.1:p.Asp344Gly
ENST00000368089.3:c.1031A>G ENSP00000357068.3:p.Asp344Gly
ENST00000509700.1:n.462+332A>G
NM_002241.4:c.1031A>G NP_002232.2:p.Asp344Gly
NM_002241.5:c.1031A>G MANE Select NP_002232.2:p.Asp344Gly