Canonical Allele Identifier: CA2008253174

Gene: KCNJ5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128891806_128891808delinsCTG , CM000673.2:g.128891806_128891808delinsCTG	GRCh38
NC_000011.9:g.128761701_128761703delinsCTG , CM000673.1:g.128761701_128761703delinsCTG	GRCh37
NC_000011.8:g.128266911_128266913delinsCTG	NCBI36
NG_023406.2:g.5389_5391delinsCTG , LRG_333:g.5389_5391delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.-11+85_-11+87delinsCTG MANE Select	ENSP00000433295.1:n.-11+85_-11+87delinsCTG
ENST00000338350.4:c.-100+85_-100+87delinsCTG	ENSP00000339960.4:n.-100+85_-100+87delinsCTG
ENST00000529694.5:c.-11+85_-11+87delinsCTG	ENSP00000433295.1:n.-11+85_-11+87delinsCTG
NM_000890.3:c.-11+85_-11+87delinsCTG , LRG_333t1:c.-11+85_-11+87delinsCTG	NP_000881.3:n.-11+85_-11+87delinsCTG
NM_000890.4:c.-11+85_-11+87delinsCTG	NP_000881.3:n.-11+85_-11+87delinsCTG
NM_001354169.1:c.-100+85_-100+87delinsCTG	NP_001341098.1:n.-100+85_-100+87delinsCTG
NM_000890.5:c.-11+85_-11+87delinsCTG MANE Select	NP_000881.3:n.-11+85_-11+87delinsCTG
NM_001354169.2:c.-100+85_-100+87delinsCTG	NP_001341098.1:n.-100+85_-100+87delinsCTG