Canonical Allele Identifier: CA2616776155

Gene: KCNJ5

Linked Data

• gnomAD v4: 11-128916740-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128916740G>T , CM000673.2:g.128916740G>T	GRCh38
NC_000011.9:g.128786635G>T , CM000673.1:g.128786635G>T	GRCh37
NC_000011.8:g.128291845G>T	NCBI36
NG_023406.2:g.30323G>T , LRG_333:g.30323G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.*9G>T MANE Select	ENSP00000433295.1:n.*9G>T
ENST00000338350.4:c.*9G>T	ENSP00000339960.4:n.*9G>T
ENST00000529694.5:c.*9G>T	ENSP00000433295.1:n.*9G>T
NM_000890.3:c.*9G>T , LRG_333t1:c.*9G>T	NP_000881.3:n.*9G>T
XM_011542809.1:c.*9G>T	XP_011541111.1:n.*9G>T
XM_011542810.1:c.*9G>T	XP_011541112.1:n.*9G>T
NM_000890.4:c.*9G>T	NP_000881.3:n.*9G>T
NM_001354169.1:c.*9G>T	NP_001341098.1:n.*9G>T
XM_011542809.2:c.*9G>T	XP_011541111.1:n.*9G>T
XM_011542810.3:c.*9G>T	XP_011541112.1:n.*9G>T
NM_000890.5:c.*9G>T MANE Select	NP_000881.3:n.*9G>T
NM_001354169.2:c.*9G>T	NP_001341098.1:n.*9G>T