Canonical Allele Identifier: CA1202156622
Gene: KCNJ10 HGNC NCBI

Linked Data

dbSNP Id: rs1571265011

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160041321G>A , CM000663.2:g.160041321G>A GRCh38
NC_000001.10:g.160011111G>A , CM000663.1:g.160011111G>A GRCh37
NC_000001.9:g.158277735G>A NCBI36
NG_016411.1:g.33851C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.671+513C>T
ENST00000636689.1:n.95-1973C>T
ENST00000637644.1:c.487+725C>T ENSP00000490282.1:n.487+725C>T
ENST00000638728.1:c.*72C>T ENSP00000492619.1:n.*72C>T
ENST00000638840.1:c.919+15C>T
ENST00000638868.1:c.*72C>T ENSP00000491250.1:n.*72C>T
ENST00000639408.1:c.488-720C>T ENSP00000491635.1:n.488-720C>T
ENST00000640017.1:c.669+513C>T ENSP00000491337.1:n.669+513C>T
ENST00000640914.1:c.124+513C>T
ENST00000644903.1:c.*72C>T MANE Select ENSP00000495557.1:n.*72C>T
ENST00000368089.3:c.*72C>T ENSP00000357068.3:n.*72C>T
ENST00000509700.1:n.462+513C>T
NM_002241.4:c.*72C>T NP_002232.2:n.*72C>T
NM_002241.5:c.*72C>T MANE Select NP_002232.2:n.*72C>T