Canonical Allele Identifier: CA1202156530
Gene: KCNJ10 HGNC NCBI

Linked Data

dbSNP Id: rs1648588399

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160041110C>T , CM000663.2:g.160041110C>T GRCh38
NC_000001.10:g.160010900C>T , CM000663.1:g.160010900C>T GRCh37
NC_000001.9:g.158277524C>T NCBI36
NG_016411.1:g.34062G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.671+724G>A
ENST00000636689.1:n.95-1762G>A
ENST00000637644.1:c.487+936G>A ENSP00000490282.1:n.487+936G>A
ENST00000638728.1:c.*283G>A ENSP00000492619.1:n.*283G>A
ENST00000638840.1:c.919+226G>A
ENST00000638868.1:c.*283G>A ENSP00000491250.1:n.*283G>A
ENST00000639408.1:c.488-509G>A ENSP00000491635.1:n.488-509G>A
ENST00000640017.1:c.670-509G>A ENSP00000491337.1:n.670-509G>A
ENST00000640914.1:c.125-509G>A
ENST00000644903.1:c.*283G>A MANE Select ENSP00000495557.1:n.*283G>A
ENST00000368089.3:c.*283G>A ENSP00000357068.3:n.*283G>A
ENST00000509700.1:n.463-509G>A
NM_002241.4:c.*283G>A NP_002232.2:n.*283G>A
NM_002241.5:c.*283G>A MANE Select NP_002232.2:n.*283G>A