Canonical Allele Identifier: CA2725211382

Gene: KCNJ5

Linked Data

• dbSNP Id: rs2136003722

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128916360_128916371del , CM000673.2:g.128916360_128916371del	GRCh38
NC_000011.9:g.128786255_128786266del , CM000673.1:g.128786255_128786266del	GRCh37
NC_000011.8:g.128291465_128291476del	NCBI36
NG_023406.2:g.29943_29954del , LRG_333:g.29943_29954del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.938-49_938-38del MANE Select	ENSP00000433295.1:n.938-49_938-38del
ENST00000338350.4:c.938-49_938-38del	ENSP00000339960.4:n.938-49_938-38del
ENST00000529694.5:c.938-49_938-38del	ENSP00000433295.1:n.938-49_938-38del
ENST00000533599.1:c.938-49_938-38del	ENSP00000434266.1:n.938-49_938-38del
NM_000890.3:c.938-49_938-38del , LRG_333t1:c.938-49_938-38del	NP_000881.3:n.938-49_938-38del
XM_011542809.1:c.938-49_938-38del	XP_011541111.1:n.938-49_938-38del
XM_011542810.1:c.938-49_938-38del	XP_011541112.1:n.938-49_938-38del
NM_000890.4:c.938-49_938-38del	NP_000881.3:n.938-49_938-38del
NM_001354169.1:c.938-49_938-38del	NP_001341098.1:n.938-49_938-38del
XM_011542809.2:c.938-49_938-38del	XP_011541111.1:n.938-49_938-38del
XM_011542810.3:c.938-49_938-38del	XP_011541112.1:n.938-49_938-38del
NM_000890.5:c.938-49_938-38del MANE Select	NP_000881.3:n.938-49_938-38del
NM_001354169.2:c.938-49_938-38del	NP_001341098.1:n.938-49_938-38del