Canonical Allele Identifier: CA31469630

Gene: KCNJ10

Linked Data

• dbSNP Id: rs961700784
• gnomAD v3: 1-160041147-T-G
• gnomAD v4: 1-160041147-T-G
• MyVariant Identifiers: chr1:g.160010937T>G (hg19) ; chr1:g.160041147T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041147T>G , CM000663.2:g.160041147T>G	GRCh38
NC_000001.10:g.160010937T>G , CM000663.1:g.160010937T>G	GRCh37
NC_000001.9:g.158277561T>G	NCBI36
NG_016411.1:g.34025A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+687A>C
ENST00000636689.1:n.95-1799A>C
ENST00000637644.1:c.487+899A>C	ENSP00000490282.1:n.487+899A>C
ENST00000638728.1:c.*246A>C	ENSP00000492619.1:n.*246A>C
ENST00000638840.1:c.919+189A>C
ENST00000638868.1:c.*246A>C	ENSP00000491250.1:n.*246A>C
ENST00000639408.1:c.488-546A>C	ENSP00000491635.1:n.488-546A>C
ENST00000640017.1:c.670-546A>C	ENSP00000491337.1:n.670-546A>C
ENST00000640914.1:c.125-546A>C
ENST00000644903.1:c.*246A>C MANE Select	ENSP00000495557.1:n.*246A>C
ENST00000368089.3:c.*246A>C	ENSP00000357068.3:n.*246A>C
ENST00000509700.1:n.463-546A>C
NM_002241.4:c.*246A>C	NP_002232.2:n.*246A>C
NM_002241.5:c.*246A>C MANE Select	NP_002232.2:n.*246A>C