Canonical Allele Identifier: CA943430770
Gene: KCNJ5 HGNC NCBI

Linked Data

dbSNP Id: rs1944582267

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128916333dup , CM000673.2:g.128916333dup GRCh38
NC_000011.9:g.128786228dup , CM000673.1:g.128786228dup GRCh37
NC_000011.8:g.128291438dup NCBI36
NG_023406.2:g.29916dup , LRG_333:g.29916dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000529694.6:c.938-76dup MANE Select ENSP00000433295.1:n.938-76dup
ENST00000338350.4:c.938-76dup ENSP00000339960.4:n.938-76dup
ENST00000529694.5:c.938-76dup ENSP00000433295.1:n.938-76dup
ENST00000533599.1:c.938-76dup ENSP00000434266.1:n.938-76dup
NM_000890.3:c.938-76dup , LRG_333t1:c.938-76dup NP_000881.3:n.938-76dup
XM_011542809.1:c.938-76dup XP_011541111.1:n.938-76dup
XM_011542810.1:c.938-76dup XP_011541112.1:n.938-76dup
NM_000890.4:c.938-76dup NP_000881.3:n.938-76dup
NM_001354169.1:c.938-76dup NP_001341098.1:n.938-76dup
XM_011542809.2:c.938-76dup XP_011541111.1:n.938-76dup
XM_011542810.3:c.938-76dup XP_011541112.1:n.938-76dup
NM_000890.5:c.938-76dup MANE Select NP_000881.3:n.938-76dup
NM_001354169.2:c.938-76dup NP_001341098.1:n.938-76dup