Canonical Allele Identifier: CA2008280058
Gene: KCNJ5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128911350C= , CM000673.2:g.128911350C= GRCh38
NC_000011.9:g.128781245C= , CM000673.1:g.128781245C= GRCh37
NC_000011.8:g.128286455C= NCBI36
NG_023406.2:g.24933C= , LRG_333:g.24933C=

Transcript Alleles

HGVS Amino-acid change
ENST00000529694.6:c.77C= MANE Select ENSP00000433295.1:p.Pro26=
ENST00000338350.4:c.77C= ENSP00000339960.4:p.Pro26=
ENST00000529694.5:c.77C= ENSP00000433295.1:p.Pro26=
ENST00000533599.1:c.77C= ENSP00000434266.1:p.Pro26=
NM_000890.3:c.77C= , LRG_333t1:c.77C= NP_000881.3:p.Pro26=
XM_011542809.1:c.77C= XP_011541111.1:p.Pro26=
XM_011542810.1:c.77C= XP_011541112.1:p.Pro26=
NM_000890.4:c.77C= NP_000881.3:p.Pro26=
NM_001354169.1:c.77C= NP_001341098.1:p.Pro26=
XM_011542809.2:c.77C= XP_011541111.1:p.Pro26=
XM_011542810.3:c.77C= XP_011541112.1:p.Pro26=
NM_000890.5:c.77C= MANE Select NP_000881.3:p.Pro26=
NM_001354169.2:c.77C= NP_001341098.1:p.Pro26=