Canonical Allele Identifier: CA343221737
Gene: KCNJ10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160041406A>T , CM000663.2:g.160041406A>T GRCh38
NC_000001.10:g.160011196A>T , CM000663.1:g.160011196A>T GRCh37
NC_000001.9:g.158277820A>T NCBI36
NG_016411.1:g.33766T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.671+428T>A
ENST00000636689.1:n.95-2058T>A
ENST00000637644.1:c.487+640T>A ENSP00000490282.1:n.487+640T>A
ENST00000638728.1:c.1127T>A ENSP00000492619.1:p.Ile376Asn
ENST00000638840.1:c.849T>A
ENST00000638868.1:c.1127T>A ENSP00000491250.1:p.Ile376Asn
ENST00000639408.1:c.487+640T>A ENSP00000491635.1:n.487+640T>A
ENST00000640017.1:c.669+428T>A ENSP00000491337.1:n.669+428T>A
ENST00000640914.1:c.124+428T>A
ENST00000644903.1:c.1127T>A MANE Select ENSP00000495557.1:p.Ile376Asn
ENST00000368089.3:c.1127T>A ENSP00000357068.3:p.Ile376Asn
ENST00000509700.1:n.462+428T>A
NM_002241.4:c.1127T>A NP_002232.2:p.Ile376Asn
NM_002241.5:c.1127T>A MANE Select NP_002232.2:p.Ile376Asn