Canonical Allele Identifier: CA2008294801
Gene: KCNJ5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128916417T= , CM000673.2:g.128916417T= GRCh38
NC_000011.9:g.128786312T= , CM000673.1:g.128786312T= GRCh37
NC_000011.8:g.128291522T= NCBI36
NG_023406.2:g.30000T= , LRG_333:g.30000T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000529694.6:c.946T= MANE Select ENSP00000433295.1:p.Cys316=
ENST00000338350.4:c.946T= ENSP00000339960.4:p.Cys316=
ENST00000529694.5:c.946T= ENSP00000433295.1:p.Cys316=
ENST00000533599.1:c.946T= ENSP00000434266.1:p.Cys316=
NM_000890.3:c.946T= , LRG_333t1:c.946T= NP_000881.3:p.Cys316=
XM_011542809.1:c.946T= XP_011541111.1:p.Cys316=
XM_011542810.1:c.946T= XP_011541112.1:p.Cys316=
NM_000890.4:c.946T= NP_000881.3:p.Cys316=
NM_001354169.1:c.946T= NP_001341098.1:p.Cys316=
XM_011542809.2:c.946T= XP_011541111.1:p.Cys316=
XM_011542810.3:c.946T= XP_011541112.1:p.Cys316=
NM_000890.5:c.946T= MANE Select NP_000881.3:p.Cys316=
NM_001354169.2:c.946T= NP_001341098.1:p.Cys316=