Canonical Allele Identifier: CA2648631416

Gene: KCNJ10

Linked Data

• gnomAD v4: 1-160040992-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160040992A>G , CM000663.2:g.160040992A>G	GRCh38
NC_000001.10:g.160010782A>G , CM000663.1:g.160010782A>G	GRCh37
NC_000001.9:g.158277406A>G	NCBI36
NG_016411.1:g.34180T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+842T>C
ENST00000636689.1:n.95-1644T>C
ENST00000637644.1:c.487+1054T>C	ENSP00000490282.1:n.487+1054T>C
ENST00000638728.1:c.*401T>C	ENSP00000492619.1:n.*401T>C
ENST00000638840.1:c.919+344T>C
ENST00000638868.1:c.*401T>C	ENSP00000491250.1:n.*401T>C
ENST00000639408.1:c.488-391T>C	ENSP00000491635.1:n.488-391T>C
ENST00000640017.1:c.670-391T>C	ENSP00000491337.1:n.670-391T>C
ENST00000640914.1:c.125-391T>C
ENST00000644903.1:c.*401T>C MANE Select	ENSP00000495557.1:n.*401T>C
ENST00000368089.3:c.*401T>C	ENSP00000357068.3:n.*401T>C
ENST00000509700.1:n.463-391T>C
NM_002241.4:c.*401T>C	NP_002232.2:n.*401T>C
NM_002241.5:c.*401T>C MANE Select	NP_002232.2:n.*401T>C