Canonical Allele Identifier: CA2648631708
Gene: KCNJ10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160041319del , CM000663.2:g.160041319del GRCh38
NC_000001.10:g.160011109del , CM000663.1:g.160011109del GRCh37
NC_000001.9:g.158277733del NCBI36
NG_016411.1:g.33855del

Transcript Alleles

HGVS Amino-acid change
ENST00000509700.2:c.671+517del
ENST00000636689.1:n.95-1969del
ENST00000637644.1:c.487+729del ENSP00000490282.1:n.487+729del
ENST00000638728.1:c.*76del ENSP00000492619.1:n.*76del
ENST00000638840.1:c.919+19del
ENST00000638868.1:c.*76del ENSP00000491250.1:n.*76del
ENST00000639408.1:c.488-716del ENSP00000491635.1:n.488-716del
ENST00000640017.1:c.669+517del ENSP00000491337.1:n.669+517del
ENST00000640914.1:c.124+517del
ENST00000644903.1:c.*76del MANE Select ENSP00000495557.1:n.*76del
ENST00000368089.3:c.*76del ENSP00000357068.3:n.*76del
ENST00000509700.1:n.462+517del
NM_002241.4:c.*76del NP_002232.2:n.*76del
NM_002241.5:c.*76del MANE Select NP_002232.2:n.*76del