Canonical Allele Identifier: CA890089758

Gene: KCNJ10

Linked Data

• dbSNP Id: rs1296188932
• gnomAD v4: 1-160041149-T-TC
• MyVariant Identifiers: chr1:g.160010939_160010940insC (hg19) ; chr1:g.160041149_160041150insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041154dup , CM000663.2:g.160041154dup	GRCh38
NC_000001.10:g.160010944dup , CM000663.1:g.160010944dup	GRCh37
NC_000001.9:g.158277568dup	NCBI36
NG_016411.1:g.34022dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+684dup
ENST00000636689.1:n.95-1802dup
ENST00000637644.1:c.487+896dup	ENSP00000490282.1:n.487+896dup
ENST00000638728.1:c.*243dup	ENSP00000492619.1:n.*243dup
ENST00000638840.1:c.919+186dup
ENST00000638868.1:c.*243dup	ENSP00000491250.1:n.*243dup
ENST00000639408.1:c.488-549dup	ENSP00000491635.1:n.488-549dup
ENST00000640017.1:c.670-549dup	ENSP00000491337.1:n.670-549dup
ENST00000640914.1:c.125-549dup
ENST00000644903.1:c.*243dup MANE Select	ENSP00000495557.1:n.*243dup
ENST00000368089.3:c.*243dup	ENSP00000357068.3:n.*243dup
ENST00000509700.1:n.463-549dup
NM_002241.4:c.*243dup	NP_002232.2:n.*243dup
NM_002241.5:c.*243dup MANE Select	NP_002232.2:n.*243dup