Canonical Allele Identifier: CA2838819383
Gene: KCNJ5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128912082_128912083insG , CM000673.2:g.128912082_128912083insG GRCh38
NC_000011.9:g.128781977_128781978insG , CM000673.1:g.128781977_128781978insG GRCh37
NC_000011.8:g.128287187_128287188insG NCBI36
NG_023406.2:g.25665_25666insG , LRG_333:g.25665_25666insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000529694.6:c.809_810insG MANE Select ENSP00000433295.1:p.Val271CysfsTer9
ENST00000338350.4:c.809_810insG ENSP00000339960.4:p.Val271CysfsTer9
ENST00000529694.5:c.809_810insG ENSP00000433295.1:p.Val271CysfsTer9
ENST00000533599.1:c.809_810insG ENSP00000434266.1:p.Val271CysfsTer9
NM_000890.3:c.809_810insG , LRG_333t1:c.809_810insG NP_000881.3:p.Val271CysfsTer9
XM_011542809.1:c.809_810insG XP_011541111.1:p.Val271CysfsTer9
XM_011542810.1:c.809_810insG XP_011541112.1:p.Val271CysfsTer9
NM_000890.4:c.809_810insG NP_000881.3:p.Val271CysfsTer9
NM_001354169.1:c.809_810insG NP_001341098.1:p.Val271CysfsTer9
XM_011542809.2:c.809_810insG XP_011541111.1:p.Val271CysfsTer9
XM_011542810.3:c.809_810insG XP_011541112.1:p.Val271CysfsTer9
NM_000890.5:c.809_810insG MANE Select NP_000881.3:p.Val271CysfsTer9
NM_001354169.2:c.809_810insG NP_001341098.1:p.Val271CysfsTer9