Canonical Allele Identifier: CA1752409631

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951517C= , CM000669.2:g.150951517C=	GRCh38
NC_000007.13:g.150648605C= , CM000669.1:g.150648605C=	GRCh37
NC_000007.12:g.150279538C=	NCBI36
NG_008916.1:g.31410G= , LRG_288:g.31410G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1174G=
ENST00000684241.1:n.2709G=
ENST00000262186.10:c.1876G= MANE Select	ENSP00000262186.5:p.Gly626=
ENST00000330883.9:c.856G=	ENSP00000328531.4:p.Gly286=
ENST00000262186.9:c.1876G=	ENSP00000262186.5:p.Gly626=
ENST00000330883.8:c.856G=	ENSP00000328531.4:p.Gly286=
ENST00000430723.4:c.1528G=	ENSP00000387657.4:p.Gly510=
ENST00000461280.1:n.1163G=
ENST00000473610.5:n.1181G=
ENST00000532957.5:n.2099G=
NM_000238.3:c.1876G= , LRG_288t1:c.1876G=	NP_000229.1:p.Gly626=
NM_001204798.1:c.856G=	NP_001191727.1:p.Gly286=
NM_172056.2:c.1876G= , LRG_288t2:c.1876G=	NP_742053.1:p.Gly626=
NM_172057.2:c.856G= , LRG_288t3:c.856G=	NP_742054.1:p.Gly286=
XM_011516185.1:c.1576G=	XP_011514487.1:p.Gly526=
XM_011516186.1:c.1876G=	XP_011514488.1:p.Gly626=
XM_011516185.2:c.1576G=	XP_011514487.1:p.Gly526=
XM_011516186.3:c.1876G=	XP_011514488.1:p.Gly626=
XM_017012195.1:c.1726G=	XP_016867684.1:p.Gly576=
XM_017012196.1:c.1699G=	XP_016867685.1:p.Gly567=
NM_000238.4:c.1876G= MANE Select	NP_000229.1:p.Gly626=
NM_001204798.2:c.856G=	NP_001191727.1:p.Gly286=
NM_172057.3:c.856G=	NP_742054.1:p.Gly286=