Canonical Allele Identifier: CA1202156512

Gene: KCNJ10

Linked Data

• dbSNP Id: rs1648587096
• gnomAD v4: 1-160041052-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041057del , CM000663.2:g.160041057del	GRCh38
NC_000001.10:g.160010847del , CM000663.1:g.160010847del	GRCh37
NC_000001.9:g.158277471del	NCBI36
NG_016411.1:g.34119del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+781del
ENST00000636689.1:n.95-1705del
ENST00000637644.1:c.487+993del	ENSP00000490282.1:n.487+993del
ENST00000638728.1:c.*340del	ENSP00000492619.1:n.*340del
ENST00000638840.1:c.919+283del
ENST00000638868.1:c.*340del	ENSP00000491250.1:n.*340del
ENST00000639408.1:c.488-452del	ENSP00000491635.1:n.488-452del
ENST00000640017.1:c.670-452del	ENSP00000491337.1:n.670-452del
ENST00000640914.1:c.125-452del
ENST00000644903.1:c.*340del MANE Select	ENSP00000495557.1:n.*340del
ENST00000368089.3:c.*340del	ENSP00000357068.3:n.*340del
ENST00000509700.1:n.463-452del
NM_002241.4:c.*340del	NP_002232.2:n.*340del
NM_002241.5:c.*340del MANE Select	NP_002232.2:n.*340del