Canonical Allele Identifier: CA1008314932

Gene: KCNJ10

Linked Data

• dbSNP Id: rs1648592347
• gnomAD v3: 1-160041244-C-G
• gnomAD v4: 1-160041244-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041244C>G , CM000663.2:g.160041244C>G	GRCh38
NC_000001.10:g.160011034C>G , CM000663.1:g.160011034C>G	GRCh37
NC_000001.9:g.158277658C>G	NCBI36
NG_016411.1:g.33928G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+590G>C
ENST00000636689.1:n.95-1896G>C
ENST00000637644.1:c.487+802G>C	ENSP00000490282.1:n.487+802G>C
ENST00000638728.1:c.*149G>C	ENSP00000492619.1:n.*149G>C
ENST00000638840.1:c.919+92G>C
ENST00000638868.1:c.*149G>C	ENSP00000491250.1:n.*149G>C
ENST00000639408.1:c.488-643G>C	ENSP00000491635.1:n.488-643G>C
ENST00000640017.1:c.669+590G>C	ENSP00000491337.1:n.669+590G>C
ENST00000640914.1:c.124+590G>C
ENST00000644903.1:c.*149G>C MANE Select	ENSP00000495557.1:n.*149G>C
ENST00000368089.3:c.*149G>C	ENSP00000357068.3:n.*149G>C
ENST00000509700.1:n.462+590G>C
NM_002241.4:c.*149G>C	NP_002232.2:n.*149G>C
NM_002241.5:c.*149G>C MANE Select	NP_002232.2:n.*149G>C