Canonical Allele Identifier: CA383250179
Gene: KCNJ5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128912057G>C , CM000673.2:g.128912057G>C GRCh38
NC_000011.9:g.128781952G>C , CM000673.1:g.128781952G>C GRCh37
NC_000011.8:g.128287162G>C NCBI36
NG_023406.2:g.25640G>C , LRG_333:g.25640G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000529694.6:c.784G>C MANE Select ENSP00000433295.1:p.Asp262His
ENST00000338350.4:c.784G>C ENSP00000339960.4:p.Asp262His
ENST00000529694.5:c.784G>C ENSP00000433295.1:p.Asp262His
ENST00000533599.1:c.784G>C ENSP00000434266.1:p.Asp262His
NM_000890.3:c.784G>C , LRG_333t1:c.784G>C NP_000881.3:p.Asp262His
XM_011542809.1:c.784G>C XP_011541111.1:p.Asp262His
XM_011542810.1:c.784G>C XP_011541112.1:p.Asp262His
NM_000890.4:c.784G>C NP_000881.3:p.Asp262His
NM_001354169.1:c.784G>C NP_001341098.1:p.Asp262His
XM_011542809.2:c.784G>C XP_011541111.1:p.Asp262His
XM_011542810.3:c.784G>C XP_011541112.1:p.Asp262His
NM_000890.5:c.784G>C MANE Select NP_000881.3:p.Asp262His
NM_001354169.2:c.784G>C NP_001341098.1:p.Asp262His