Canonical Allele Identifier: CA421597891
Gene: KCNJ10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160012251C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160042461C>T , CM000663.2:g.160042461C>T GRCh38
NC_000001.10:g.160012251C>T , CM000663.1:g.160012251C>T GRCh37
NC_000001.9:g.158278875C>T NCBI36
NG_016411.1:g.32711G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000509700.2:c.44G>A
ENST00000636689.1:n.95-3113G>A
ENST00000637644.1:c.72G>A ENSP00000490282.1:p.Gly24=
ENST00000638728.1:c.72G>A ENSP00000492619.1:p.Gly24=
ENST00000638868.1:c.72G>A ENSP00000491250.1:p.Gly24=
ENST00000639408.1:c.72G>A ENSP00000491635.1:p.Gly24=
ENST00000640017.1:c.42G>A ENSP00000491337.1:p.Gly14=
ENST00000644903.1:c.72G>A MANE Select ENSP00000495557.1:p.Gly24=
ENST00000368089.3:c.72G>A ENSP00000357068.3:p.Gly24=
NM_002241.4:c.72G>A NP_002232.2:p.Gly24=
NM_002241.5:c.72G>A MANE Select NP_002232.2:p.Gly24=