Canonical Allele Identifier: CA2008252685

Gene: KCNJ5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128891485_128891496delinsGCTGCTCTCGCT , CM000673.2:g.128891485_128891496delinsGCTGCTCTCGCT	GRCh38
NC_000011.9:g.128761380_128761391delinsGCTGCTCTCGCT , CM000673.1:g.128761380_128761391delinsGCTGCTCTCGCT	GRCh37
NC_000011.8:g.128266590_128266601delinsGCTGCTCTCGCT	NCBI36
NG_023406.2:g.5068_5079delinsGCTGCTCTCGCT , LRG_333:g.5068_5079delinsGCTGCTCTCGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.-247_-236delinsGCTGCTCTCGCT MANE Select	ENSP00000433295.1:n.-247_-236delinsGCTGCTCTCGCT
ENST00000338350.4:c.-336_-325delinsGCTGCTCTCGCT	ENSP00000339960.4:n.-336_-325delinsGCTGCTCTCGCT
ENST00000529694.5:c.-247_-236delinsGCTGCTCTCGCT	ENSP00000433295.1:n.-247_-236delinsGCTGCTCTCGCT
NM_000890.3:c.-247_-236delinsGCTGCTCTCGCT , LRG_333t1:c.-247_-236delinsGCTGCTCTCGCT	NP_000881.3:n.-247_-236delinsGCTGCTCTCGCT
NM_000890.4:c.-247_-236delinsGCTGCTCTCGCT	NP_000881.3:n.-247_-236delinsGCTGCTCTCGCT
NM_001354169.1:c.-336_-325delinsGCTGCTCTCGCT	NP_001341098.1:n.-336_-325delinsGCTGCTCTCGCT
NM_000890.5:c.-247_-236delinsGCTGCTCTCGCT MANE Select	NP_000881.3:n.-247_-236delinsGCTGCTCTCGCT
NM_001354169.2:c.-336_-325delinsGCTGCTCTCGCT	NP_001341098.1:n.-336_-325delinsGCTGCTCTCGCT