Canonical Allele Identifier: CA2008283074
Gene: KCNJ1 HGNC NCBI

Linked Data

dbSNP Id: rs1943800380

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128865427C>T , CM000673.2:g.128865427C>T GRCh38
NC_000011.9:g.128735322C>T , CM000673.1:g.128735322C>T GRCh37
NC_000011.8:g.128240532C>T NCBI36
NG_009379.1:g.6947G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392666.6:c.-192+1746G>A MANE Select ENSP00000376434.1:n.-192+1746G>A
ENST00000324003.3:c.-192+1746G>A ENSP00000316136.3:n.-192+1746G>A
ENST00000324036.7:c.-192+1096G>A ENSP00000316233.3:n.-192+1096G>A
ENST00000392665.6:c.-22+1746G>A ENSP00000376433.2:n.-22+1746G>A
ENST00000392666.5:c.-192+1746G>A ENSP00000376434.1:n.-192+1746G>A
ENST00000440599.6:c.-22+1096G>A ENSP00000406320.2:n.-22+1096G>A
ENST00000531562.1:n.124+1746G>A
NM_153764.2:c.-22+1746G>A NP_722448.1:n.-22+1746G>A
NM_153765.2:c.30+1096G>A NP_722449.3:n.30+1096G>A
NM_153766.2:c.-192+1746G>A NP_722450.1:n.-192+1746G>A
NM_153767.3:c.-192+1096G>A NP_722451.1:n.-192+1096G>A
XR_001748442.1:n.3533-1323C>T
NM_153764.3:c.-22+1746G>A NP_722448.1:n.-22+1746G>A
NM_153765.3:c.30+1096G>A NP_722449.3:n.30+1096G>A
NM_153766.3:c.-192+1746G>A MANE Select NP_722450.1:n.-192+1746G>A
NM_153767.4:c.-192+1096G>A NP_722451.1:n.-192+1096G>A