Canonical Allele Identifier: CA602377635

Gene: KCNJ5

Linked Data

• dbSNP Id: rs1472450066
• gnomAD v2: 11-128786041-ATATATCTTTGCCCTTTCCTGCCTTTTTTTCCATATC-A
• gnomAD v3: 11-128916146-ATATATCTTTGCCCTTTCCTGCCTTTTTTTCCATATC-A
• gnomAD v4: 11-128916146-ATATATCTTTGCCCTTTCCTGCCTTTTTTTCCATATC-A
• MyVariant Identifiers: chr11:g.128786042_128786077del (hg19) ; chr11:g.128916147_128916182del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128916148_128916183del , CM000673.2:g.128916148_128916183del	GRCh38
NC_000011.9:g.128786043_128786078del , CM000673.1:g.128786043_128786078del	GRCh37
NC_000011.8:g.128291253_128291288del	NCBI36
NG_023406.2:g.29731_29766del , LRG_333:g.29731_29766del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.938-261_938-226del MANE Select	ENSP00000433295.1:n.938-261_938-226del
ENST00000338350.4:c.938-261_938-226del	ENSP00000339960.4:n.938-261_938-226del
ENST00000529694.5:c.938-261_938-226del	ENSP00000433295.1:n.938-261_938-226del
ENST00000533599.1:c.938-261_938-226del	ENSP00000434266.1:n.938-261_938-226del
NM_000890.3:c.938-261_938-226del , LRG_333t1:c.938-261_938-226del	NP_000881.3:n.938-261_938-226del
XM_011542809.1:c.938-261_938-226del	XP_011541111.1:n.938-261_938-226del
XM_011542810.1:c.938-261_938-226del	XP_011541112.1:n.938-261_938-226del
NM_000890.4:c.938-261_938-226del	NP_000881.3:n.938-261_938-226del
NM_001354169.1:c.938-261_938-226del	NP_001341098.1:n.938-261_938-226del
XM_011542809.2:c.938-261_938-226del	XP_011541111.1:n.938-261_938-226del
XM_011542810.3:c.938-261_938-226del	XP_011541112.1:n.938-261_938-226del
NM_000890.5:c.938-261_938-226del MANE Select	NP_000881.3:n.938-261_938-226del
NM_001354169.2:c.938-261_938-226del	NP_001341098.1:n.938-261_938-226del