Canonical Allele Identifier: CA2648631541

Gene: KCNJ10

Linked Data

• gnomAD v4: 1-160041145-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160041145T>A , CM000663.2:g.160041145T>A	GRCh38
NC_000001.10:g.160010935T>A , CM000663.1:g.160010935T>A	GRCh37
NC_000001.9:g.158277559T>A	NCBI36
NG_016411.1:g.34027A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509700.2:c.671+689A>T
ENST00000636689.1:n.95-1797A>T
ENST00000637644.1:c.487+901A>T	ENSP00000490282.1:n.487+901A>T
ENST00000638728.1:c.*248A>T	ENSP00000492619.1:n.*248A>T
ENST00000638840.1:c.919+191A>T
ENST00000638868.1:c.*248A>T	ENSP00000491250.1:n.*248A>T
ENST00000639408.1:c.488-544A>T	ENSP00000491635.1:n.488-544A>T
ENST00000640017.1:c.670-544A>T	ENSP00000491337.1:n.670-544A>T
ENST00000640914.1:c.125-544A>T
ENST00000644903.1:c.*248A>T MANE Select	ENSP00000495557.1:n.*248A>T
ENST00000368089.3:c.*248A>T	ENSP00000357068.3:n.*248A>T
ENST00000509700.1:n.463-544A>T
NM_002241.4:c.*248A>T	NP_002232.2:n.*248A>T
NM_002241.5:c.*248A>T MANE Select	NP_002232.2:n.*248A>T