Canonical Allele Identifier: CA2008292584
Community Standard Title: NM_000890.5(KCNJ5):c.452G= (p.Gly151=)
Gene: KCNJ5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128911725G= , CM000673.2:g.128911725G= GRCh38
NC_000011.9:g.128781620G= , CM000673.1:g.128781620G= GRCh37
NC_000011.8:g.128286830G= NCBI36
NG_023406.2:g.25308G= , LRG_333:g.25308G=

Transcript Alleles

HGVS Amino-acid Change
NM_000890.5:c.452G= MANE Select NP_000881.3:p.Gly151=
ENST00000529694.6:c.452G= MANE Select ENSP00000433295.1:p.Gly151=
NM_000890.3:c.452G= , LRG_333t1:c.452G= NP_000881.3:p.Gly151=
NM_000890.4:c.452G= NP_000881.3:p.Gly151=
NM_001354169.1:c.452G= NP_001341098.1:p.Gly151=
NM_001354169.2:c.452G= NP_001341098.1:p.Gly151=
ENST00000338350.4:c.452G= ENSP00000339960.4:p.Gly151=
ENST00000529694.5:c.452G= ENSP00000433295.1:p.Gly151=
ENST00000533599.1:c.452G= ENSP00000434266.1:p.Gly151=
XM_011542809.1:c.452G= XP_011541111.1:p.Gly151=
XM_011542809.2:c.452G= XP_011541111.1:p.Gly151=
XM_011542810.1:c.452G= XP_011541112.1:p.Gly151=
XM_011542810.3:c.452G= XP_011541112.1:p.Gly151=