Canonical Allele Identifier: CA1193177

Gene: KCNJ10

Linked Data

• dbSNP Id: rs756827951
• ExAC: 1:160011303 A / C
• gnomAD v2: 1-160011303-A-C
• gnomAD v3: 1-160041513-A-C
• gnomAD v4: 1-160041513-A-C
• MyVariant Identifiers: chr1:g.160011303A>C (hg19) ; chr1:g.160041513A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041513A>C , CM000663.2:g.160041513A>C	GRCh38
NC_000001.10:g.160011303A>C , CM000663.1:g.160011303A>C	GRCh37
NC_000001.9:g.158277927A>C	NCBI36
NG_016411.1:g.33659T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+321T>G
ENST00000636689.1:n.95-2165T>G
ENST00000637644.1:c.487+533T>G	ENSP00000490282.1:n.487+533T>G
ENST00000638728.1:c.1020T>G	ENSP00000492619.1:p.Ser340Arg
ENST00000638840.1:c.742T>G
ENST00000638868.1:c.1020T>G	ENSP00000491250.1:p.Ser340Arg
ENST00000639408.1:c.487+533T>G	ENSP00000491635.1:n.487+533T>G
ENST00000640017.1:c.669+321T>G	ENSP00000491337.1:n.669+321T>G
ENST00000640914.1:c.124+321T>G
ENST00000644903.1:c.1020T>G MANE Select	ENSP00000495557.1:p.Ser340Arg
ENST00000368089.3:c.1020T>G	ENSP00000357068.3:p.Ser340Arg
ENST00000509700.1:n.462+321T>G
NM_002241.4:c.1020T>G	NP_002232.2:p.Ser340Arg
NM_002241.5:c.1020T>G MANE Select	NP_002232.2:p.Ser340Arg