Canonical Allele Identifier: CA31469446

Gene: KCNJ10

Linked Data

• dbSNP Id: rs1049083650
• gnomAD v3: 1-160040951-A-G
• gnomAD v4: 1-160040951-A-G
• MyVariant Identifiers: chr1:g.160010741A>G (hg19) ; chr1:g.160040951A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160040951A>G , CM000663.2:g.160040951A>G	GRCh38
NC_000001.10:g.160010741A>G , CM000663.1:g.160010741A>G	GRCh37
NC_000001.9:g.158277365A>G	NCBI36
NG_016411.1:g.34221T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+883T>C
ENST00000636689.1:n.95-1603T>C
ENST00000637644.1:c.487+1095T>C	ENSP00000490282.1:n.487+1095T>C
ENST00000638728.1:c.*442T>C	ENSP00000492619.1:n.*442T>C
ENST00000638840.1:c.920-350T>C
ENST00000638868.1:c.*442T>C	ENSP00000491250.1:n.*442T>C
ENST00000639408.1:c.488-350T>C	ENSP00000491635.1:n.488-350T>C
ENST00000640017.1:c.670-350T>C	ENSP00000491337.1:n.670-350T>C
ENST00000640914.1:c.125-350T>C
ENST00000644903.1:c.*442T>C MANE Select	ENSP00000495557.1:n.*442T>C
ENST00000368089.3:c.*442T>C	ENSP00000357068.3:n.*442T>C
ENST00000509700.1:n.463-350T>C
NM_002241.4:c.*442T>C	NP_002232.2:n.*442T>C
NM_002241.5:c.*442T>C MANE Select	NP_002232.2:n.*442T>C