Canonical Allele Identifier: CA1202156471
Gene: KCNJ10 HGNC NCBI

Linked Data

dbSNP Id: rs1648585000

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160040948G>C , CM000663.2:g.160040948G>C GRCh38
NC_000001.10:g.160010738G>C , CM000663.1:g.160010738G>C GRCh37
NC_000001.9:g.158277362G>C NCBI36
NG_016411.1:g.34224C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.671+886C>G
ENST00000636689.1:n.95-1600C>G
ENST00000637644.1:c.487+1098C>G ENSP00000490282.1:n.487+1098C>G
ENST00000638728.1:c.*445C>G ENSP00000492619.1:n.*445C>G
ENST00000638840.1:c.920-347C>G
ENST00000638868.1:c.*445C>G ENSP00000491250.1:n.*445C>G
ENST00000639408.1:c.488-347C>G ENSP00000491635.1:n.488-347C>G
ENST00000640017.1:c.670-347C>G ENSP00000491337.1:n.670-347C>G
ENST00000640914.1:c.125-347C>G
ENST00000644903.1:c.*445C>G MANE Select ENSP00000495557.1:n.*445C>G
ENST00000368089.3:c.*445C>G ENSP00000357068.3:n.*445C>G
ENST00000509700.1:n.463-347C>G
NM_002241.4:c.*445C>G NP_002232.2:n.*445C>G
NM_002241.5:c.*445C>G MANE Select NP_002232.2:n.*445C>G