Canonical Allele Identifier: CA2746335992
Gene: KCNJ10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160041402del , CM000663.2:g.160041402del GRCh38
NC_000001.10:g.160011192del , CM000663.1:g.160011192del GRCh37
NC_000001.9:g.158277816del NCBI36
NG_016411.1:g.33770del

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.671+432del
ENST00000636689.1:n.95-2054del
ENST00000637644.1:c.487+644del ENSP00000490282.1:n.487+644del
ENST00000638728.1:c.1131del ENSP00000492619.1:p.Ser377ArgfsTer24
ENST00000638840.1:c.853del
ENST00000638868.1:c.1131del ENSP00000491250.1:p.Ser377ArgfsTer24
ENST00000639408.1:c.487+644del ENSP00000491635.1:n.487+644del
ENST00000640017.1:c.669+432del ENSP00000491337.1:n.669+432del
ENST00000640914.1:c.124+432del
ENST00000644903.1:c.1131del MANE Select ENSP00000495557.1:p.Ser377ArgfsTer24
ENST00000368089.3:c.1131del ENSP00000357068.3:p.Ser377ArgfsTer24
ENST00000509700.1:n.462+432del
NM_002241.4:c.1131del NP_002232.2:p.Ser377ArgfsTer24
NM_002241.5:c.1131del MANE Select NP_002232.2:p.Ser377ArgfsTer24