Canonical Allele Identifier: CA383235414

Gene: KCNJ5

Linked Data

• MyVariant Identifiers: chr11:g.128786357C>G (hg19) ; chr11:g.128916462C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128916462C>G , CM000673.2:g.128916462C>G	GRCh38
NC_000011.9:g.128786357C>G , CM000673.1:g.128786357C>G	GRCh37
NC_000011.8:g.128291567C>G	NCBI36
NG_023406.2:g.30045C>G , LRG_333:g.30045C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.991C>G MANE Select	ENSP00000433295.1:p.His331Asp
ENST00000338350.4:c.991C>G	ENSP00000339960.4:p.His331Asp
ENST00000529694.5:c.991C>G	ENSP00000433295.1:p.His331Asp
ENST00000533599.1:c.991C>G	ENSP00000434266.1:p.His331Asp
NM_000890.3:c.991C>G , LRG_333t1:c.991C>G	NP_000881.3:p.His331Asp
XM_011542809.1:c.991C>G	XP_011541111.1:p.His331Asp
XM_011542810.1:c.991C>G	XP_011541112.1:p.His331Asp
NM_000890.4:c.991C>G	NP_000881.3:p.His331Asp
NM_001354169.1:c.991C>G	NP_001341098.1:p.His331Asp
XM_011542809.2:c.991C>G	XP_011541111.1:p.His331Asp
XM_011542810.3:c.991C>G	XP_011541112.1:p.His331Asp
NM_000890.5:c.991C>G MANE Select	NP_000881.3:p.His331Asp
NM_001354169.2:c.991C>G	NP_001341098.1:p.His331Asp