Canonical Allele Identifier: CA2521800997

Gene: KCNJ10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041530del , CM000663.2:g.160041530del	GRCh38
NC_000001.10:g.160011320del , CM000663.1:g.160011320del	GRCh37
NC_000001.9:g.158277944del	NCBI36
NG_016411.1:g.33644del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+306del
ENST00000636689.1:n.95-2180del
ENST00000637644.1:c.487+518del	ENSP00000490282.1:n.487+518del
ENST00000638728.1:c.1005del	ENSP00000492619.1:p.Val336TrpfsTer26
ENST00000638840.1:c.727del
ENST00000638868.1:c.1005del	ENSP00000491250.1:p.Val336TrpfsTer26
ENST00000639408.1:c.487+518del	ENSP00000491635.1:n.487+518del
ENST00000640017.1:c.669+306del	ENSP00000491337.1:n.669+306del
ENST00000640914.1:c.124+306del
ENST00000644903.1:c.1005del MANE Select	ENSP00000495557.1:p.Val336TrpfsTer26
ENST00000368089.3:c.1005del	ENSP00000357068.3:p.Val336TrpfsTer26
ENST00000509700.1:n.462+306del
NM_002241.4:c.1005del	NP_002232.2:p.Val336TrpfsTer26
NM_002241.5:c.1005del MANE Select	NP_002232.2:p.Val336TrpfsTer26