Canonical Allele Identifier: CA2648631707
Gene: KCNJ10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160041316del , CM000663.2:g.160041316del GRCh38
NC_000001.10:g.160011106del , CM000663.1:g.160011106del GRCh37
NC_000001.9:g.158277730del NCBI36
NG_016411.1:g.33858del

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.671+520del
ENST00000636689.1:n.95-1966del
ENST00000637644.1:c.487+732del ENSP00000490282.1:n.487+732del
ENST00000638728.1:c.*79del ENSP00000492619.1:n.*79del
ENST00000638840.1:c.919+22del
ENST00000638868.1:c.*79del ENSP00000491250.1:n.*79del
ENST00000639408.1:c.488-713del ENSP00000491635.1:n.488-713del
ENST00000640017.1:c.669+520del ENSP00000491337.1:n.669+520del
ENST00000640914.1:c.124+520del
ENST00000644903.1:c.*79del MANE Select ENSP00000495557.1:n.*79del
ENST00000368089.3:c.*79del ENSP00000357068.3:n.*79del
ENST00000509700.1:n.462+520del
NM_002241.4:c.*79del NP_002232.2:n.*79del
NM_002241.5:c.*79del MANE Select NP_002232.2:n.*79del