Canonical Allele Identifier: CA2843280604

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041303_160041304del , CM000663.2:g.160041303_160041304del	GRCh38
NC_000001.10:g.160011093_160011094del , CM000663.1:g.160011093_160011094del	GRCh37
NC_000001.9:g.158277717_158277718del	NCBI36
NG_016411.1:g.33871_33872del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+533_671+534del
ENST00000636689.1:n.95-1953_95-1952del
ENST00000637644.1:c.487+745_487+746del	ENSP00000490282.1:n.487+745_487+746del
ENST00000638728.1:c.*92_*93del	ENSP00000492619.1:n.*92_*93del
ENST00000638840.1:c.919+35_919+36del
ENST00000638868.1:c.*92_*93del	ENSP00000491250.1:n.*92_*93del
ENST00000639408.1:c.488-700_488-699del	ENSP00000491635.1:n.488-700_488-699del
ENST00000640017.1:c.669+533_669+534del	ENSP00000491337.1:n.669+533_669+534del
ENST00000640914.1:c.124+533_124+534del
ENST00000644903.1:c.*92_*93del MANE Select	ENSP00000495557.1:n.*92_*93del
ENST00000368089.3:c.*92_*93del	ENSP00000357068.3:n.*92_*93del
ENST00000509700.1:n.462+533_462+534del
NM_002241.4:c.*92_*93del	NP_002232.2:n.*92_*93del
NM_002241.5:c.*92_*93del MANE Select	NP_002232.2:n.*92_*93del