Canonical Allele Identifier: CA2008253069

Gene: KCNJ5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128891734_128891735delinsCT , CM000673.2:g.128891734_128891735delinsCT	GRCh38
NC_000011.9:g.128761629_128761630delinsCT , CM000673.1:g.128761629_128761630delinsCT	GRCh37
NC_000011.8:g.128266839_128266840delinsCT	NCBI36
NG_023406.2:g.5317_5318delinsCT , LRG_333:g.5317_5318delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.-11+13_-11+14delinsCT MANE Select	ENSP00000433295.1:n.-11+13_-11+14delinsCT
ENST00000338350.4:c.-100+13_-100+14delinsCT	ENSP00000339960.4:n.-100+13_-100+14delinsCT
ENST00000529694.5:c.-11+13_-11+14delinsCT	ENSP00000433295.1:n.-11+13_-11+14delinsCT
NM_000890.3:c.-11+13_-11+14delinsCT , LRG_333t1:c.-11+13_-11+14delinsCT	NP_000881.3:n.-11+13_-11+14delinsCT
NM_000890.4:c.-11+13_-11+14delinsCT	NP_000881.3:n.-11+13_-11+14delinsCT
NM_001354169.1:c.-100+13_-100+14delinsCT	NP_001341098.1:n.-100+13_-100+14delinsCT
NM_000890.5:c.-11+13_-11+14delinsCT MANE Select	NP_000881.3:n.-11+13_-11+14delinsCT
NM_001354169.2:c.-100+13_-100+14delinsCT	NP_001341098.1:n.-100+13_-100+14delinsCT