Canonical Allele Identifier: CA1202156469

Gene: KCNJ10

Linked Data

• dbSNP Id: rs1648584956
• gnomAD v4: 1-160040947-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160040947A>C , CM000663.2:g.160040947A>C	GRCh38
NC_000001.10:g.160010737A>C , CM000663.1:g.160010737A>C	GRCh37
NC_000001.9:g.158277361A>C	NCBI36
NG_016411.1:g.34225T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+887T>G
ENST00000636689.1:n.95-1599T>G
ENST00000637644.1:c.487+1099T>G	ENSP00000490282.1:n.487+1099T>G
ENST00000638728.1:c.*446T>G	ENSP00000492619.1:n.*446T>G
ENST00000638840.1:c.920-346T>G
ENST00000638868.1:c.*446T>G	ENSP00000491250.1:n.*446T>G
ENST00000639408.1:c.488-346T>G	ENSP00000491635.1:n.488-346T>G
ENST00000640017.1:c.670-346T>G	ENSP00000491337.1:n.670-346T>G
ENST00000640914.1:c.125-346T>G
ENST00000644903.1:c.*446T>G MANE Select	ENSP00000495557.1:n.*446T>G
ENST00000368089.3:c.*446T>G	ENSP00000357068.3:n.*446T>G
ENST00000509700.1:n.463-346T>G
NM_002241.4:c.*446T>G	NP_002232.2:n.*446T>G
NM_002241.5:c.*446T>G MANE Select	NP_002232.2:n.*446T>G