Canonical Allele Identifier: CA31469462

Gene: KCNJ10

Linked Data

• dbSNP Id: rs546202393
• MyVariant Identifiers: chr1:g.160010742C>T (hg19) ; chr1:g.160040952C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160040952C>T , CM000663.2:g.160040952C>T	GRCh38
NC_000001.10:g.160010742C>T , CM000663.1:g.160010742C>T	GRCh37
NC_000001.9:g.158277366C>T	NCBI36
NG_016411.1:g.34220G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+882G>A
ENST00000636689.1:n.95-1604G>A
ENST00000637644.1:c.487+1094G>A	ENSP00000490282.1:n.487+1094G>A
ENST00000638728.1:c.*441G>A	ENSP00000492619.1:n.*441G>A
ENST00000638840.1:c.920-351G>A
ENST00000638868.1:c.*441G>A	ENSP00000491250.1:n.*441G>A
ENST00000639408.1:c.488-351G>A	ENSP00000491635.1:n.488-351G>A
ENST00000640017.1:c.670-351G>A	ENSP00000491337.1:n.670-351G>A
ENST00000640914.1:c.125-351G>A
ENST00000644903.1:c.*441G>A MANE Select	ENSP00000495557.1:n.*441G>A
ENST00000368089.3:c.*441G>A	ENSP00000357068.3:n.*441G>A
ENST00000509700.1:n.463-351G>A
NM_002241.4:c.*441G>A	NP_002232.2:n.*441G>A
NM_002241.5:c.*441G>A MANE Select	NP_002232.2:n.*441G>A