Canonical Allele Identifier: CA1202156545
Gene: KCNJ10 HGNC NCBI

Linked Data

dbSNP Id: rs1648589087

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160041149dup , CM000663.2:g.160041149dup GRCh38
NC_000001.10:g.160010939dup , CM000663.1:g.160010939dup GRCh37
NC_000001.9:g.158277563dup NCBI36
NG_016411.1:g.34025dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.671+687dup
ENST00000636689.1:n.95-1799dup
ENST00000637644.1:c.487+899dup ENSP00000490282.1:n.487+899dup
ENST00000638728.1:c.*246dup ENSP00000492619.1:n.*246dup
ENST00000638840.1:c.919+189dup
ENST00000638868.1:c.*246dup ENSP00000491250.1:n.*246dup
ENST00000639408.1:c.488-546dup ENSP00000491635.1:n.488-546dup
ENST00000640017.1:c.670-546dup ENSP00000491337.1:n.670-546dup
ENST00000640914.1:c.125-546dup
ENST00000644903.1:c.*246dup MANE Select ENSP00000495557.1:n.*246dup
ENST00000368089.3:c.*246dup ENSP00000357068.3:n.*246dup
ENST00000509700.1:n.463-546dup
NM_002241.4:c.*246dup NP_002232.2:n.*246dup
NM_002241.5:c.*246dup MANE Select NP_002232.2:n.*246dup