Canonical Allele Identifier: CA602377629

Gene: KCNJ5

Linked Data

• dbSNP Id: rs56658633
• gnomAD v2: 11-128785997-TTGGATGGATGGA-T
• gnomAD v3: 11-128916102-TTGGATGGATGGA-T
• gnomAD v4: 11-128916102-TTGGATGGATGGA-T
• MyVariant Identifiers: chr11:g.128786002_128786013del (hg19) ; chr11:g.128785998_128786009del (hg19) ; chr11:g.128916107_128916118del (hg38) ; chr11:g.128916103_128916114del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128916136_128916147del , CM000673.2:g.128916136_128916147del	GRCh38
NC_000011.9:g.128786031_128786042del , CM000673.1:g.128786031_128786042del	GRCh37
NC_000011.8:g.128291241_128291252del	NCBI36
NG_023406.2:g.29719_29730del , LRG_333:g.29719_29730del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.938-273_938-262del MANE Select	ENSP00000433295.1:n.938-273_938-262del
ENST00000338350.4:c.938-273_938-262del	ENSP00000339960.4:n.938-273_938-262del
ENST00000529694.5:c.938-273_938-262del	ENSP00000433295.1:n.938-273_938-262del
ENST00000533599.1:c.938-273_938-262del	ENSP00000434266.1:n.938-273_938-262del
NM_000890.3:c.938-273_938-262del , LRG_333t1:c.938-273_938-262del	NP_000881.3:n.938-273_938-262del
XM_011542809.1:c.938-273_938-262del	XP_011541111.1:n.938-273_938-262del
XM_011542810.1:c.938-273_938-262del	XP_011541112.1:n.938-273_938-262del
NM_000890.4:c.938-273_938-262del	NP_000881.3:n.938-273_938-262del
NM_001354169.1:c.938-273_938-262del	NP_001341098.1:n.938-273_938-262del
XM_011542809.2:c.938-273_938-262del	XP_011541111.1:n.938-273_938-262del
XM_011542810.3:c.938-273_938-262del	XP_011541112.1:n.938-273_938-262del
NM_000890.5:c.938-273_938-262del MANE Select	NP_000881.3:n.938-273_938-262del
NM_001354169.2:c.938-273_938-262del	NP_001341098.1:n.938-273_938-262del