Canonical Allele Identifier: CA31469444

Gene: KCNJ10

Linked Data

• dbSNP Id: rs748563412
• gnomAD v3: 1-160040946-A-G
• gnomAD v4: 1-160040946-A-G
• MyVariant Identifiers: chr1:g.160010736A>G (hg19) ; chr1:g.160040946A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160040946A>G , CM000663.2:g.160040946A>G	GRCh38
NC_000001.10:g.160010736A>G , CM000663.1:g.160010736A>G	GRCh37
NC_000001.9:g.158277360A>G	NCBI36
NG_016411.1:g.34226T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+888T>C
ENST00000636689.1:n.95-1598T>C
ENST00000637644.1:c.487+1100T>C	ENSP00000490282.1:n.487+1100T>C
ENST00000638728.1:c.*447T>C	ENSP00000492619.1:n.*447T>C
ENST00000638840.1:c.920-345T>C
ENST00000638868.1:c.*447T>C	ENSP00000491250.1:n.*447T>C
ENST00000639408.1:c.488-345T>C	ENSP00000491635.1:n.488-345T>C
ENST00000640017.1:c.670-345T>C	ENSP00000491337.1:n.670-345T>C
ENST00000640914.1:c.125-345T>C
ENST00000644903.1:c.*447T>C MANE Select	ENSP00000495557.1:n.*447T>C
ENST00000368089.3:c.*447T>C	ENSP00000357068.3:n.*447T>C
ENST00000509700.1:n.463-345T>C
NM_002241.4:c.*447T>C	NP_002232.2:n.*447T>C
NM_002241.5:c.*447T>C MANE Select	NP_002232.2:n.*447T>C