Canonical Allele Identifier: CA602585904
Gene: KCNJ5 HGNC NCBI

Linked Data

dbSNP Id: rs1261023408
gnomAD v2: 11-128786185-C-CTGGA
gnomAD v3: 11-128916290-C-CTGGA
gnomAD v4: 11-128916290-C-CTGGA
MyVariant Identifiers: chr11:g.128786189_128786190insTGGA (hg19) chr11:g.128786185_128786186insTGGA (hg19) chr11:g.128916294_128916295insTGGA (hg38) chr11:g.128916290_128916291insTGGA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128916308_128916311dup , CM000673.2:g.128916308_128916311dup GRCh38
NC_000011.9:g.128786203_128786206dup , CM000673.1:g.128786203_128786206dup GRCh37
NC_000011.8:g.128291413_128291416dup NCBI36
NG_023406.2:g.29891_29894dup , LRG_333:g.29891_29894dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000529694.6:c.938-101_938-98dup MANE Select ENSP00000433295.1:n.938-101_938-98dup
ENST00000338350.4:c.938-101_938-98dup ENSP00000339960.4:n.938-101_938-98dup
ENST00000529694.5:c.938-101_938-98dup ENSP00000433295.1:n.938-101_938-98dup
ENST00000533599.1:c.938-101_938-98dup ENSP00000434266.1:n.938-101_938-98dup
NM_000890.3:c.938-101_938-98dup , LRG_333t1:c.938-101_938-98dup NP_000881.3:n.938-101_938-98dup
XM_011542809.1:c.938-101_938-98dup XP_011541111.1:n.938-101_938-98dup
XM_011542810.1:c.938-101_938-98dup XP_011541112.1:n.938-101_938-98dup
NM_000890.4:c.938-101_938-98dup NP_000881.3:n.938-101_938-98dup
NM_001354169.1:c.938-101_938-98dup NP_001341098.1:n.938-101_938-98dup
XM_011542809.2:c.938-101_938-98dup XP_011541111.1:n.938-101_938-98dup
XM_011542810.3:c.938-101_938-98dup XP_011541112.1:n.938-101_938-98dup
NM_000890.5:c.938-101_938-98dup MANE Select NP_000881.3:n.938-101_938-98dup
NM_001354169.2:c.938-101_938-98dup NP_001341098.1:n.938-101_938-98dup
Search 100 bp 5'
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