Canonical Allele Identifier: CA10630386

Gene: KCNJ5

Linked Data

• ClinVar Variation Id: 303590
• ClinVar RCV Id: RCV000266866 ; RCV000363821
• dbSNP Id: rs886047990
• MyVariant Identifiers: chr11:g.128761326_128761336delinsGAGAGAGAGAGAGAG (hg19) ; chr11:g.128891431_128891441delinsGAGAGAGAGAGAGAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128891431_128891441delinsGAGAGAGAGAGAGAG , CM000673.2:g.128891431_128891441delinsGAGAGAGAGAGAGAG	GRCh38
NC_000011.9:g.128761326_128761336delinsGAGAGAGAGAGAGAG , CM000673.1:g.128761326_128761336delinsGAGAGAGAGAGAGAG	GRCh37
NC_000011.8:g.128266536_128266546delinsGAGAGAGAGAGAGAG	NCBI36
NG_023406.2:g.5014_5024delinsGAGAGAGAGAGAGAG , LRG_333:g.5014_5024delinsGAGAGAGAGAGAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.-301_-291delinsGAGAGAGAGAGAGAG MANE Select	ENSP00000433295.1:n.-301_-291delinsGAGAGAGAGAGAGAG
ENST00000529694.5:c.-301_-291delinsGAGAGAGAGAGAGAG	ENSP00000433295.1:n.-301_-291delinsGAGAGAGAGAGAGAG
NM_000890.3:c.-301_-291delinsGAGAGAGAGAGAGAG , LRG_333t1:c.-301_-291delinsGAGAGAGAGAGAGAG	NP_000881.3:n.-301_-291delinsGAGAGAGAGAGAGAG
NM_000890.4:c.-301_-291delinsGAGAGAGAGAGAGAG	NP_000881.3:n.-301_-291delinsGAGAGAGAGAGAGAG
NM_001354169.1:c.-390_-380delinsGAGAGAGAGAGAGAG	NP_001341098.1:n.-390_-380delinsGAGAGAGAGAGAGAG
NM_000890.5:c.-301_-291delinsGAGAGAGAGAGAGAG MANE Select	NP_000881.3:n.-301_-291delinsGAGAGAGAGAGAGAG
NM_001354169.2:c.-390_-380delinsGAGAGAGAGAGAGAG	NP_001341098.1:n.-390_-380delinsGAGAGAGAGAGAGAG