Canonical Allele Identifier: CA2616775777
Gene: KCNJ5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128916308_128916309insACTG , CM000673.2:g.128916308_128916309insACTG GRCh38
NC_000011.9:g.128786203_128786204insACTG , CM000673.1:g.128786203_128786204insACTG GRCh37
NC_000011.8:g.128291413_128291414insACTG NCBI36
NG_023406.2:g.29891_29892insACTG , LRG_333:g.29891_29892insACTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000529694.6:c.938-101_938-100insACTG MANE Select ENSP00000433295.1:n.938-101_938-100insACTG
ENST00000338350.4:c.938-101_938-100insACTG ENSP00000339960.4:n.938-101_938-100insACTG
ENST00000529694.5:c.938-101_938-100insACTG ENSP00000433295.1:n.938-101_938-100insACTG
ENST00000533599.1:c.938-101_938-100insACTG ENSP00000434266.1:n.938-101_938-100insACTG
NM_000890.3:c.938-101_938-100insACTG , LRG_333t1:c.938-101_938-100insACTG NP_000881.3:n.938-101_938-100insACTG
XM_011542809.1:c.938-101_938-100insACTG XP_011541111.1:n.938-101_938-100insACTG
XM_011542810.1:c.938-101_938-100insACTG XP_011541112.1:n.938-101_938-100insACTG
NM_000890.4:c.938-101_938-100insACTG NP_000881.3:n.938-101_938-100insACTG
NM_001354169.1:c.938-101_938-100insACTG NP_001341098.1:n.938-101_938-100insACTG
XM_011542809.2:c.938-101_938-100insACTG XP_011541111.1:n.938-101_938-100insACTG
XM_011542810.3:c.938-101_938-100insACTG XP_011541112.1:n.938-101_938-100insACTG
NM_000890.5:c.938-101_938-100insACTG MANE Select NP_000881.3:n.938-101_938-100insACTG
NM_001354169.2:c.938-101_938-100insACTG NP_001341098.1:n.938-101_938-100insACTG