Canonical Allele Identifier: CA383246906
Gene: KCNJ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128840065T>A , CM000673.2:g.128840065T>A GRCh38
NC_000011.9:g.128709960T>A , CM000673.1:g.128709960T>A GRCh37
NC_000011.8:g.128215170T>A NCBI36
NG_009379.1:g.32309A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392666.6:c.179A>T MANE Select ENSP00000376434.1:p.Tyr60Phe
ENST00000324003.3:c.179A>T ENSP00000316136.3:p.Tyr60Phe
ENST00000324036.7:c.179A>T ENSP00000316233.3:p.Tyr60Phe
ENST00000392664.2:c.236A>T ENSP00000376432.2:p.Tyr79Phe
ENST00000392665.6:c.179A>T ENSP00000376433.2:p.Tyr60Phe
ENST00000392666.5:c.179A>T ENSP00000376434.1:p.Tyr60Phe
ENST00000440599.6:c.179A>T ENSP00000406320.2:p.Tyr60Phe
ENST00000531562.1:n.524A>T
NM_000220.4:c.236A>T NP_000211.1:p.Tyr79Phe
NM_153764.2:c.179A>T NP_722448.1:p.Tyr60Phe
NM_153765.2:c.230A>T NP_722449.3:p.Tyr77Phe
NM_153766.2:c.179A>T NP_722450.1:p.Tyr60Phe
NM_153767.3:c.179A>T NP_722451.1:p.Tyr60Phe
NM_000220.6:c.236A>T NP_000211.1:p.Tyr79Phe
NM_153764.3:c.179A>T NP_722448.1:p.Tyr60Phe
NM_153765.3:c.230A>T NP_722449.3:p.Tyr77Phe
NM_153766.3:c.179A>T MANE Select NP_722450.1:p.Tyr60Phe
NM_153767.4:c.179A>T NP_722451.1:p.Tyr60Phe