Canonical Allele Identifier: CA2616776190

Gene: KCNJ5

Linked Data

• gnomAD v4: 11-128916761-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128916761A>G , CM000673.2:g.128916761A>G	GRCh38
NC_000011.9:g.128786656A>G , CM000673.1:g.128786656A>G	GRCh37
NC_000011.8:g.128291866A>G	NCBI36
NG_023406.2:g.30344A>G , LRG_333:g.30344A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.*30A>G MANE Select	ENSP00000433295.1:n.*30A>G
ENST00000338350.4:c.*30A>G	ENSP00000339960.4:n.*30A>G
ENST00000529694.5:c.*30A>G	ENSP00000433295.1:n.*30A>G
NM_000890.3:c.*30A>G , LRG_333t1:c.*30A>G	NP_000881.3:n.*30A>G
XM_011542809.1:c.*30A>G	XP_011541111.1:n.*30A>G
XM_011542810.1:c.*30A>G	XP_011541112.1:n.*30A>G
NM_000890.4:c.*30A>G	NP_000881.3:n.*30A>G
NM_001354169.1:c.*30A>G	NP_001341098.1:n.*30A>G
XM_011542809.2:c.*30A>G	XP_011541111.1:n.*30A>G
XM_011542810.3:c.*30A>G	XP_011541112.1:n.*30A>G
NM_000890.5:c.*30A>G MANE Select	NP_000881.3:n.*30A>G
NM_001354169.2:c.*30A>G	NP_001341098.1:n.*30A>G