Canonical Allele Identifier: CA230627329
Gene: KCNJ1 HGNC NCBI

Linked Data

dbSNP Id: rs1055570758

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128839003T>C , CM000673.2:g.128839003T>C GRCh38
NC_000011.9:g.128708898T>C , CM000673.1:g.128708898T>C GRCh37
NC_000011.8:g.128214108T>C NCBI36
NG_009379.1:g.33371A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000392666.6:c.*122A>G MANE Select ENSP00000376434.1:n.*122A>G
ENST00000324036.7:c.*122A>G ENSP00000316233.3:n.*122A>G
ENST00000392664.2:c.*122A>G ENSP00000376432.2:n.*122A>G
ENST00000392665.6:c.*122A>G ENSP00000376433.2:n.*122A>G
ENST00000392666.5:c.*122A>G ENSP00000376434.1:n.*122A>G
ENST00000440599.6:c.*122A>G ENSP00000406320.2:n.*122A>G
NM_000220.4:c.*122A>G NP_000211.1:n.*122A>G
NM_153764.2:c.*122A>G NP_722448.1:n.*122A>G
NM_153765.2:c.*122A>G NP_722449.3:n.*122A>G
NM_153766.2:c.*122A>G NP_722450.1:n.*122A>G
NM_153767.3:c.*122A>G NP_722451.1:n.*122A>G
NM_000220.6:c.*122A>G NP_000211.1:n.*122A>G
NM_153764.3:c.*122A>G NP_722448.1:n.*122A>G
NM_153765.3:c.*122A>G NP_722449.3:n.*122A>G
NM_153766.3:c.*122A>G MANE Select NP_722450.1:n.*122A>G
NM_153767.4:c.*122A>G NP_722451.1:n.*122A>G