Canonical Allele Identifier: CA2008253078

Gene: KCNJ5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128891737_128891740delinsTTCC , CM000673.2:g.128891737_128891740delinsTTCC	GRCh38
NC_000011.9:g.128761632_128761635delinsTTCC , CM000673.1:g.128761632_128761635delinsTTCC	GRCh37
NC_000011.8:g.128266842_128266845delinsTTCC	NCBI36
NG_023406.2:g.5320_5323delinsTTCC , LRG_333:g.5320_5323delinsTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.-11+16_-11+19delinsTTCC MANE Select	ENSP00000433295.1:n.-11+16_-11+19delinsTTCC
ENST00000338350.4:c.-100+16_-100+19delinsTTCC	ENSP00000339960.4:n.-100+16_-100+19delinsTTCC
ENST00000529694.5:c.-11+16_-11+19delinsTTCC	ENSP00000433295.1:n.-11+16_-11+19delinsTTCC
NM_000890.3:c.-11+16_-11+19delinsTTCC , LRG_333t1:c.-11+16_-11+19delinsTTCC	NP_000881.3:n.-11+16_-11+19delinsTTCC
NM_000890.4:c.-11+16_-11+19delinsTTCC	NP_000881.3:n.-11+16_-11+19delinsTTCC
NM_001354169.1:c.-100+16_-100+19delinsTTCC	NP_001341098.1:n.-100+16_-100+19delinsTTCC
NM_000890.5:c.-11+16_-11+19delinsTTCC MANE Select	NP_000881.3:n.-11+16_-11+19delinsTTCC
NM_001354169.2:c.-100+16_-100+19delinsTTCC	NP_001341098.1:n.-100+16_-100+19delinsTTCC