Canonical Allele Identifier: CA2575025437
Gene: KCNJ5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128916627_128916628insAG , CM000673.2:g.128916627_128916628insAG GRCh38
NC_000011.9:g.128786522_128786523insAG , CM000673.1:g.128786522_128786523insAG GRCh37
NC_000011.8:g.128291732_128291733insAG NCBI36
NG_023406.2:g.30210_30211insAG , LRG_333:g.30210_30211insAG

Transcript Alleles

HGVS Amino-acid change
ENST00000529694.6:c.1156_1157insAG MANE Select ENSP00000433295.1:p.Leu386GlnfsTer?
ENST00000338350.4:c.1156_1157insAG ENSP00000339960.4:p.Leu386GlnfsTer?
ENST00000529694.5:c.1156_1157insAG ENSP00000433295.1:p.Leu386GlnfsTer?
ENST00000533599.1:c.1156_1157insAG ENSP00000434266.1:p.Leu386GlnfsTer?
NM_000890.3:c.1156_1157insAG , LRG_333t1:c.1156_1157insAG NP_000881.3:p.Leu386GlnfsTer?
XM_011542809.1:c.1156_1157insAG XP_011541111.1:p.Leu386GlnfsTer?
XM_011542810.1:c.1156_1157insAG XP_011541112.1:p.Leu386GlnfsTer?
NM_000890.4:c.1156_1157insAG NP_000881.3:p.Leu386GlnfsTer?
NM_001354169.1:c.1156_1157insAG NP_001341098.1:p.Leu386GlnfsTer?
XM_011542809.2:c.1156_1157insAG XP_011541111.1:p.Leu386GlnfsTer?
XM_011542810.3:c.1156_1157insAG XP_011541112.1:p.Leu386GlnfsTer?
NM_000890.5:c.1156_1157insAG MANE Select NP_000881.3:p.Leu386GlnfsTer?
NM_001354169.2:c.1156_1157insAG NP_001341098.1:p.Leu386GlnfsTer?