Canonical Allele Identifier: CA1008314964
Gene: KCNJ10 HGNC NCBI

Linked Data

dbSNP Id: rs115130978

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160041304G>C , CM000663.2:g.160041304G>C GRCh38
NC_000001.10:g.160011094G>C , CM000663.1:g.160011094G>C GRCh37
NC_000001.9:g.158277718G>C NCBI36
NG_016411.1:g.33868C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000509700.2:c.671+530C>G
ENST00000636689.1:n.95-1956C>G
ENST00000637644.1:c.487+742C>G ENSP00000490282.1:n.487+742C>G
ENST00000638728.1:c.*89C>G ENSP00000492619.1:n.*89C>G
ENST00000638840.1:c.919+32C>G
ENST00000638868.1:c.*89C>G ENSP00000491250.1:n.*89C>G
ENST00000639408.1:c.488-703C>G ENSP00000491635.1:n.488-703C>G
ENST00000640017.1:c.669+530C>G ENSP00000491337.1:n.669+530C>G
ENST00000640914.1:c.124+530C>G
ENST00000644903.1:c.*89C>G MANE Select ENSP00000495557.1:n.*89C>G
ENST00000368089.3:c.*89C>G ENSP00000357068.3:n.*89C>G
ENST00000509700.1:n.462+530C>G
NM_002241.4:c.*89C>G NP_002232.2:n.*89C>G
NM_002241.5:c.*89C>G MANE Select NP_002232.2:n.*89C>G