Canonical Allele Identifier: CA1008314871

Gene: KCNJ10

Linked Data

• dbSNP Id: rs1648585332
• gnomAD v3: 1-160040964-G-T
• gnomAD v4: 1-160040964-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160040964G>T , CM000663.2:g.160040964G>T	GRCh38
NC_000001.10:g.160010754G>T , CM000663.1:g.160010754G>T	GRCh37
NC_000001.9:g.158277378G>T	NCBI36
NG_016411.1:g.34208C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+870C>A
ENST00000636689.1:n.95-1616C>A
ENST00000637644.1:c.487+1082C>A	ENSP00000490282.1:n.487+1082C>A
ENST00000638728.1:c.*429C>A	ENSP00000492619.1:n.*429C>A
ENST00000638840.1:c.920-363C>A
ENST00000638868.1:c.*429C>A	ENSP00000491250.1:n.*429C>A
ENST00000639408.1:c.488-363C>A	ENSP00000491635.1:n.488-363C>A
ENST00000640017.1:c.670-363C>A	ENSP00000491337.1:n.670-363C>A
ENST00000640914.1:c.125-363C>A
ENST00000644903.1:c.*429C>A MANE Select	ENSP00000495557.1:n.*429C>A
ENST00000368089.3:c.*429C>A	ENSP00000357068.3:n.*429C>A
ENST00000509700.1:n.463-363C>A
NM_002241.4:c.*429C>A	NP_002232.2:n.*429C>A
NM_002241.5:c.*429C>A MANE Select	NP_002232.2:n.*429C>A