Canonical Allele Identifier: CA1202156475
Gene: KCNJ10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160040969G= , CM000663.2:g.160040969G= GRCh38
NC_000001.10:g.160010759G= , CM000663.1:g.160010759G= GRCh37
NC_000001.9:g.158277383G= NCBI36
NG_016411.1:g.34203C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.671+865C=
ENST00000636689.1:n.95-1621C=
ENST00000637644.1:c.487+1077C= ENSP00000490282.1:n.487+1077C=
ENST00000638728.1:c.*424C= ENSP00000492619.1:n.*424C=
ENST00000638840.1:c.920-368C=
ENST00000638868.1:c.*424C= ENSP00000491250.1:n.*424C=
ENST00000639408.1:c.488-368C= ENSP00000491635.1:n.488-368C=
ENST00000640017.1:c.670-368C= ENSP00000491337.1:n.670-368C=
ENST00000640914.1:c.125-368C=
ENST00000644903.1:c.*424C= MANE Select ENSP00000495557.1:n.*424C=
ENST00000368089.3:c.*424C= ENSP00000357068.3:n.*424C=
ENST00000509700.1:n.463-368C=
NM_002241.4:c.*424C= NP_002232.2:n.*424C=
NM_002241.5:c.*424C= MANE Select NP_002232.2:n.*424C=