Canonical Allele Identifier: CA6357555
Gene: KCNJ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2573381
ClinVar RCV Id: RCV003317717
dbSNP Id: rs189845122

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128840047A>T , CM000673.2:g.128840047A>T GRCh38
NC_000011.9:g.128709942A>T , CM000673.1:g.128709942A>T GRCh37
NC_000011.8:g.128215152A>T NCBI36
NG_009379.1:g.32327T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392666.6:c.197T>A MANE Select ENSP00000376434.1:p.Ile66Asn
ENST00000324003.3:c.197T>A ENSP00000316136.3:p.Ile66Asn
ENST00000324036.7:c.197T>A ENSP00000316233.3:p.Ile66Asn
ENST00000392664.2:c.254T>A ENSP00000376432.2:p.Ile85Asn
ENST00000392665.6:c.197T>A ENSP00000376433.2:p.Ile66Asn
ENST00000392666.5:c.197T>A ENSP00000376434.1:p.Ile66Asn
ENST00000440599.6:c.197T>A ENSP00000406320.2:p.Ile66Asn
NM_000220.4:c.254T>A NP_000211.1:p.Ile85Asn
NM_153764.2:c.197T>A NP_722448.1:p.Ile66Asn
NM_153765.2:c.248T>A NP_722449.3:p.Ile83Asn
NM_153766.2:c.197T>A NP_722450.1:p.Ile66Asn
NM_153767.3:c.197T>A NP_722451.1:p.Ile66Asn
NM_000220.6:c.254T>A NP_000211.1:p.Ile85Asn
NM_153764.3:c.197T>A NP_722448.1:p.Ile66Asn
NM_153765.3:c.248T>A NP_722449.3:p.Ile83Asn
NM_153766.3:c.197T>A MANE Select NP_722450.1:p.Ile66Asn
NM_153767.4:c.197T>A NP_722451.1:p.Ile66Asn