Canonical Allele Identifier: CA31469645

Gene: KCNJ10

Linked Data

• dbSNP Id: rs1030158376
• gnomAD v2: 1-160010949-TG-T
• gnomAD v3: 1-160041159-TG-T
• gnomAD v4: 1-160041159-TG-T
• MyVariant Identifiers: chr1:g.160010950del (hg19) ; chr1:g.160041160del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041161del , CM000663.2:g.160041161del	GRCh38
NC_000001.10:g.160010951del , CM000663.1:g.160010951del	GRCh37
NC_000001.9:g.158277575del	NCBI36
NG_016411.1:g.34012del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+674del
ENST00000636689.1:n.95-1812del
ENST00000637644.1:c.487+886del	ENSP00000490282.1:n.487+886del
ENST00000638728.1:c.*233del	ENSP00000492619.1:n.*233del
ENST00000638840.1:c.919+176del
ENST00000638868.1:c.*233del	ENSP00000491250.1:n.*233del
ENST00000639408.1:c.488-559del	ENSP00000491635.1:n.488-559del
ENST00000640017.1:c.670-559del	ENSP00000491337.1:n.670-559del
ENST00000640914.1:c.125-559del
ENST00000644903.1:c.*233del MANE Select	ENSP00000495557.1:n.*233del
ENST00000368089.3:c.*233del	ENSP00000357068.3:n.*233del
ENST00000509700.1:n.463-559del
NM_002241.4:c.*233del	NP_002232.2:n.*233del
NM_002241.5:c.*233del MANE Select	NP_002232.2:n.*233del