Canonical Allele Identifier: CA1202156502

Gene: KCNJ10

Linked Data

• dbSNP Id: rs1010735588
• gnomAD v4: 1-160041040-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041040G>T , CM000663.2:g.160041040G>T	GRCh38
NC_000001.10:g.160010830G>T , CM000663.1:g.160010830G>T	GRCh37
NC_000001.9:g.158277454G>T	NCBI36
NG_016411.1:g.34132C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+794C>A
ENST00000636689.1:n.95-1692C>A
ENST00000637644.1:c.487+1006C>A	ENSP00000490282.1:n.487+1006C>A
ENST00000638728.1:c.*353C>A	ENSP00000492619.1:n.*353C>A
ENST00000638840.1:c.919+296C>A
ENST00000638868.1:c.*353C>A	ENSP00000491250.1:n.*353C>A
ENST00000639408.1:c.488-439C>A	ENSP00000491635.1:n.488-439C>A
ENST00000640017.1:c.670-439C>A	ENSP00000491337.1:n.670-439C>A
ENST00000640914.1:c.125-439C>A
ENST00000644903.1:c.*353C>A MANE Select	ENSP00000495557.1:n.*353C>A
ENST00000368089.3:c.*353C>A	ENSP00000357068.3:n.*353C>A
ENST00000509700.1:n.463-439C>A
NM_002241.4:c.*353C>A	NP_002232.2:n.*353C>A
NM_002241.5:c.*353C>A MANE Select	NP_002232.2:n.*353C>A