Canonical Allele Identifier: CA31469815

Gene: KCNJ10

Linked Data

• ClinVar Variation Id: 873572
• ClinVar RCV Id: RCV001095834 ; RCV001095833
• dbSNP Id: rs114052043
• gnomAD v2: 1-160011090-G-A
• gnomAD v3: 1-160041300-G-A
• gnomAD v4: 1-160041300-G-A
• MyVariant Identifiers: chr1:g.160011090G>A (hg19) ; chr1:g.160041300G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041300G>A , CM000663.2:g.160041300G>A	GRCh38
NC_000001.10:g.160011090G>A , CM000663.1:g.160011090G>A	GRCh37
NC_000001.9:g.158277714G>A	NCBI36
NG_016411.1:g.33872C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+534C>T
ENST00000636689.1:n.95-1952C>T
ENST00000637644.1:c.487+746C>T	ENSP00000490282.1:n.487+746C>T
ENST00000638728.1:c.*93C>T	ENSP00000492619.1:n.*93C>T
ENST00000638840.1:c.919+36C>T
ENST00000638868.1:c.*93C>T	ENSP00000491250.1:n.*93C>T
ENST00000639408.1:c.488-699C>T	ENSP00000491635.1:n.488-699C>T
ENST00000640017.1:c.669+534C>T	ENSP00000491337.1:n.669+534C>T
ENST00000640914.1:c.124+534C>T
ENST00000644903.1:c.*93C>T MANE Select	ENSP00000495557.1:n.*93C>T
ENST00000368089.3:c.*93C>T	ENSP00000357068.3:n.*93C>T
ENST00000509700.1:n.462+534C>T
NM_002241.4:c.*93C>T	NP_002232.2:n.*93C>T
NM_002241.5:c.*93C>T MANE Select	NP_002232.2:n.*93C>T