Canonical Allele Identifier: CA383246824
Gene: KCNJ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128840053A>G , CM000673.2:g.128840053A>G GRCh38
NC_000011.9:g.128709948A>G , CM000673.1:g.128709948A>G GRCh37
NC_000011.8:g.128215158A>G NCBI36
NG_009379.1:g.32321T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000392666.6:c.191T>C MANE Select ENSP00000376434.1:p.Ile64Thr
ENST00000324003.3:c.191T>C ENSP00000316136.3:p.Ile64Thr
ENST00000324036.7:c.191T>C ENSP00000316233.3:p.Ile64Thr
ENST00000392664.2:c.248T>C ENSP00000376432.2:p.Ile83Thr
ENST00000392665.6:c.191T>C ENSP00000376433.2:p.Ile64Thr
ENST00000392666.5:c.191T>C ENSP00000376434.1:p.Ile64Thr
ENST00000440599.6:c.191T>C ENSP00000406320.2:p.Ile64Thr
NM_000220.4:c.248T>C NP_000211.1:p.Ile83Thr
NM_153764.2:c.191T>C NP_722448.1:p.Ile64Thr
NM_153765.2:c.242T>C NP_722449.3:p.Ile81Thr
NM_153766.2:c.191T>C NP_722450.1:p.Ile64Thr
NM_153767.3:c.191T>C NP_722451.1:p.Ile64Thr
NM_000220.6:c.248T>C NP_000211.1:p.Ile83Thr
NM_153764.3:c.191T>C NP_722448.1:p.Ile64Thr
NM_153765.3:c.242T>C NP_722449.3:p.Ile81Thr
NM_153766.3:c.191T>C MANE Select NP_722450.1:p.Ile64Thr
NM_153767.4:c.191T>C NP_722451.1:p.Ile64Thr