Canonical Allele Identifier: CA2008293329

Gene: KCNJ5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128912117C= , CM000673.2:g.128912117C=	GRCh38
NC_000011.9:g.128782012C= , CM000673.1:g.128782012C=	GRCh37
NC_000011.8:g.128287222C=	NCBI36
NG_023406.2:g.25700C= , LRG_333:g.25700C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.844C= MANE Select	ENSP00000433295.1:p.Gln282=
ENST00000338350.4:c.844C=	ENSP00000339960.4:p.Gln282=
ENST00000529694.5:c.844C=	ENSP00000433295.1:p.Gln282=
ENST00000533599.1:c.844C=	ENSP00000434266.1:p.Gln282=
NM_000890.3:c.844C= , LRG_333t1:c.844C=	NP_000881.3:p.Gln282=
XM_011542809.1:c.844C=	XP_011541111.1:p.Gln282=
XM_011542810.1:c.844C=	XP_011541112.1:p.Gln282=
NM_000890.4:c.844C=	NP_000881.3:p.Gln282=
NM_001354169.1:c.844C=	NP_001341098.1:p.Gln282=
XM_011542809.2:c.844C=	XP_011541111.1:p.Gln282=
XM_011542810.3:c.844C=	XP_011541112.1:p.Gln282=
NM_000890.5:c.844C= MANE Select	NP_000881.3:p.Gln282=
NM_001354169.2:c.844C=	NP_001341098.1:p.Gln282=