Canonical Allele Identifier: CA1202156553

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041166_160041167delinsAG , CM000663.2:g.160041166_160041167delinsAG	GRCh38
NC_000001.10:g.160010956_160010957delinsAG , CM000663.1:g.160010956_160010957delinsAG	GRCh37
NC_000001.9:g.158277580_158277581delinsAG	NCBI36
NG_016411.1:g.34005_34006delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+667_671+668delinsCT
ENST00000636689.1:n.95-1819_95-1818delinsCT
ENST00000637644.1:c.487+879_487+880delinsCT	ENSP00000490282.1:n.487+879_487+880delinsCT
ENST00000638728.1:c.*226_*227delinsCT	ENSP00000492619.1:n.*226_*227delinsCT
ENST00000638840.1:c.919+169_919+170delinsCT
ENST00000638868.1:c.*226_*227delinsCT	ENSP00000491250.1:n.*226_*227delinsCT
ENST00000639408.1:c.488-566_488-565delinsCT	ENSP00000491635.1:n.488-566_488-565delinsCT
ENST00000640017.1:c.670-566_670-565delinsCT	ENSP00000491337.1:n.670-566_670-565delinsCT
ENST00000640914.1:c.125-566_125-565delinsCT
ENST00000644903.1:c.*226_*227delinsCT MANE Select	ENSP00000495557.1:n.*226_*227delinsCT
ENST00000368089.3:c.*226_*227delinsCT	ENSP00000357068.3:n.*226_*227delinsCT
ENST00000509700.1:n.463-566_463-565delinsCT
NM_002241.4:c.*226_*227delinsCT	NP_002232.2:n.*226_*227delinsCT
NM_002241.5:c.*226_*227delinsCT MANE Select	NP_002232.2:n.*226_*227delinsCT