Canonical Allele Identifier: CA383236036
Gene: KCNJ5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.128786525G>A (hg19) chr11:g.128916630G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128916630G>A , CM000673.2:g.128916630G>A GRCh38
NC_000011.9:g.128786525G>A , CM000673.1:g.128786525G>A GRCh37
NC_000011.8:g.128291735G>A NCBI36
NG_023406.2:g.30213G>A , LRG_333:g.30213G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000529694.6:c.1159G>A MANE Select ENSP00000433295.1:p.Gly387Arg
ENST00000338350.4:c.1159G>A ENSP00000339960.4:p.Gly387Arg
ENST00000529694.5:c.1159G>A ENSP00000433295.1:p.Gly387Arg
ENST00000533599.1:c.1159G>A ENSP00000434266.1:p.Gly387Arg
NM_000890.3:c.1159G>A , LRG_333t1:c.1159G>A NP_000881.3:p.Gly387Arg
XM_011542809.1:c.1159G>A XP_011541111.1:p.Gly387Arg
XM_011542810.1:c.1159G>A XP_011541112.1:p.Gly387Arg
NM_000890.4:c.1159G>A NP_000881.3:p.Gly387Arg
NM_001354169.1:c.1159G>A NP_001341098.1:p.Gly387Arg
XM_011542809.2:c.1159G>A XP_011541111.1:p.Gly387Arg
XM_011542810.3:c.1159G>A XP_011541112.1:p.Gly387Arg
NM_000890.5:c.1159G>A MANE Select NP_000881.3:p.Gly387Arg
NM_001354169.2:c.1159G>A NP_001341098.1:p.Gly387Arg
Search 100 bp 5'
Search 100 bp 3'