Canonical Allele Identifier: CA1144229024
Gene: KCNJ10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160042009C= , CM000663.2:g.160042009C= GRCh38
NC_000001.10:g.160011799C= , CM000663.1:g.160011799C= GRCh37
NC_000001.9:g.158278423C= NCBI36
NG_016411.1:g.33163G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.496G=
ENST00000636689.1:n.95-2661G=
ENST00000637644.1:c.487+37G= ENSP00000490282.1:n.487+37G=
ENST00000638728.1:c.524G= ENSP00000492619.1:p.Arg175=
ENST00000638840.1:c.246G=
ENST00000638868.1:c.524G= ENSP00000491250.1:p.Arg175=
ENST00000639408.1:c.487+37G= ENSP00000491635.1:n.487+37G=
ENST00000640017.1:c.494G= ENSP00000491337.1:p.Arg165=
ENST00000644903.1:c.524G= MANE Select ENSP00000495557.1:p.Arg175=
ENST00000368089.3:c.524G= ENSP00000357068.3:p.Arg175=
ENST00000509700.1:n.287G=
NM_002241.4:c.524G= NP_002232.2:p.Arg175=
NM_002241.5:c.524G= MANE Select NP_002232.2:p.Arg175=