Canonical Allele Identifier: CA343222782
Gene: KCNJ10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160041529T>A , CM000663.2:g.160041529T>A GRCh38
NC_000001.10:g.160011319T>A , CM000663.1:g.160011319T>A GRCh37
NC_000001.9:g.158277943T>A NCBI36
NG_016411.1:g.33643A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.671+305A>T
ENST00000636689.1:n.95-2181A>T
ENST00000637644.1:c.487+517A>T ENSP00000490282.1:n.487+517A>T
ENST00000638728.1:c.1004A>T ENSP00000492619.1:p.Lys335Ile
ENST00000638840.1:c.726A>T
ENST00000638868.1:c.1004A>T ENSP00000491250.1:p.Lys335Ile
ENST00000639408.1:c.487+517A>T ENSP00000491635.1:n.487+517A>T
ENST00000640017.1:c.669+305A>T ENSP00000491337.1:n.669+305A>T
ENST00000640914.1:c.124+305A>T
ENST00000644903.1:c.1004A>T MANE Select ENSP00000495557.1:p.Lys335Ile
ENST00000368089.3:c.1004A>T ENSP00000357068.3:p.Lys335Ile
ENST00000509700.1:n.462+305A>T
NM_002241.4:c.1004A>T NP_002232.2:p.Lys335Ile
NM_002241.5:c.1004A>T MANE Select NP_002232.2:p.Lys335Ile