Canonical Allele Identifier: CA2648631759
Gene: KCNJ10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160041418dup , CM000663.2:g.160041418dup GRCh38
NC_000001.10:g.160011208dup , CM000663.1:g.160011208dup GRCh37
NC_000001.9:g.158277832dup NCBI36
NG_016411.1:g.33755dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.671+417dup
ENST00000636689.1:n.95-2069dup
ENST00000637644.1:c.487+629dup ENSP00000490282.1:n.487+629dup
ENST00000638728.1:c.1116dup ENSP00000492619.1:p.Ser373Ter
ENST00000638840.1:c.838dup
ENST00000638868.1:c.1116dup ENSP00000491250.1:p.Ser373Ter
ENST00000639408.1:c.487+629dup ENSP00000491635.1:n.487+629dup
ENST00000640017.1:c.669+417dup ENSP00000491337.1:n.669+417dup
ENST00000640914.1:c.124+417dup
ENST00000644903.1:c.1116dup MANE Select ENSP00000495557.1:p.Ser373Ter
ENST00000368089.3:c.1116dup ENSP00000357068.3:p.Ser373Ter
ENST00000509700.1:n.462+417dup
NM_002241.4:c.1116dup NP_002232.2:p.Ser373Ter
NM_002241.5:c.1116dup MANE Select NP_002232.2:p.Ser373Ter