Canonical Allele Identifier: CA673278261

Gene: KCNJ5

Linked Data

• dbSNP Id: rs1276993171
• gnomAD v4: 11-128916300-GGATGGATGGATA-G
• MyVariant Identifiers: chr11:g.128786196_128786207del (hg19) ; chr11:g.128916301_128916312del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128916312_128916323del , CM000673.2:g.128916312_128916323del	GRCh38
NC_000011.9:g.128786207_128786218del , CM000673.1:g.128786207_128786218del	GRCh37
NC_000011.8:g.128291417_128291428del	NCBI36
NG_023406.2:g.29895_29906del , LRG_333:g.29895_29906del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.938-97_938-86del MANE Select	ENSP00000433295.1:n.938-97_938-86del
ENST00000338350.4:c.938-97_938-86del	ENSP00000339960.4:n.938-97_938-86del
ENST00000529694.5:c.938-97_938-86del	ENSP00000433295.1:n.938-97_938-86del
ENST00000533599.1:c.938-97_938-86del	ENSP00000434266.1:n.938-97_938-86del
NM_000890.3:c.938-97_938-86del , LRG_333t1:c.938-97_938-86del	NP_000881.3:n.938-97_938-86del
XM_011542809.1:c.938-97_938-86del	XP_011541111.1:n.938-97_938-86del
XM_011542810.1:c.938-97_938-86del	XP_011541112.1:n.938-97_938-86del
NM_000890.4:c.938-97_938-86del	NP_000881.3:n.938-97_938-86del
NM_001354169.1:c.938-97_938-86del	NP_001341098.1:n.938-97_938-86del
XM_011542809.2:c.938-97_938-86del	XP_011541111.1:n.938-97_938-86del
XM_011542810.3:c.938-97_938-86del	XP_011541112.1:n.938-97_938-86del
NM_000890.5:c.938-97_938-86del MANE Select	NP_000881.3:n.938-97_938-86del
NM_001354169.2:c.938-97_938-86del	NP_001341098.1:n.938-97_938-86del