Canonical Allele Identifier: CA1202156511

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041052_160041053delinsAG , CM000663.2:g.160041052_160041053delinsAG	GRCh38
NC_000001.10:g.160010842_160010843delinsAG , CM000663.1:g.160010842_160010843delinsAG	GRCh37
NC_000001.9:g.158277466_158277467delinsAG	NCBI36
NG_016411.1:g.34119_34120delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+781_671+782delinsCT
ENST00000636689.1:n.95-1705_95-1704delinsCT
ENST00000637644.1:c.487+993_487+994delinsCT	ENSP00000490282.1:n.487+993_487+994delinsCT
ENST00000638728.1:c.*340_*341delinsCT	ENSP00000492619.1:n.*340_*341delinsCT
ENST00000638840.1:c.919+283_919+284delinsCT
ENST00000638868.1:c.*340_*341delinsCT	ENSP00000491250.1:n.*340_*341delinsCT
ENST00000639408.1:c.488-452_488-451delinsCT	ENSP00000491635.1:n.488-452_488-451delinsCT
ENST00000640017.1:c.670-452_670-451delinsCT	ENSP00000491337.1:n.670-452_670-451delinsCT
ENST00000640914.1:c.125-452_125-451delinsCT
ENST00000644903.1:c.*340_*341delinsCT MANE Select	ENSP00000495557.1:n.*340_*341delinsCT
ENST00000368089.3:c.*340_*341delinsCT	ENSP00000357068.3:n.*340_*341delinsCT
ENST00000509700.1:n.463-452_463-451delinsCT
NM_002241.4:c.*340_*341delinsCT	NP_002232.2:n.*340_*341delinsCT
NM_002241.5:c.*340_*341delinsCT MANE Select	NP_002232.2:n.*340_*341delinsCT