Canonical Allele Identifier: CA1752432892

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950021G= , CM000669.2:g.150950021G=	GRCh38
NC_000007.13:g.150647109G= , CM000669.1:g.150647109G=	GRCh37
NC_000007.12:g.150278042G=	NCBI36
NG_008916.1:g.32906C= , LRG_288:g.32906C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1843C=
ENST00000684241.1:n.3231+147C=
ENST00000262186.10:c.2398+147C= MANE Select	ENSP00000262186.5:n.2398+147C=
ENST00000330883.9:c.1378+147C=	ENSP00000328531.4:n.1378+147C=
ENST00000262186.9:c.2398+147C=	ENSP00000262186.5:n.2398+147C=
ENST00000330883.8:c.1378+147C=	ENSP00000328531.4:n.1378+147C=
ENST00000430723.4:c.2197C=	ENSP00000387657.4:p.Pro733=
ENST00000461280.1:n.1832C=
ENST00000473610.5:n.2177C=
ENST00000532957.5:n.2768C=
NM_000238.3:c.2398+147C= , LRG_288t1:c.2398+147C=	NP_000229.1:n.2398+147C=
NM_001204798.1:c.1525C=	NP_001191727.1:p.Pro509=
NM_172056.2:c.2545C= , LRG_288t2:c.2545C=	NP_742053.1:p.Pro849=
NM_172057.2:c.1378+147C= , LRG_288t3:c.1378+147C=	NP_742054.1:n.1378+147C=
XM_011516185.1:c.2098+147C=	XP_011514487.1:n.2098+147C=
XM_011516186.1:c.2398+147C=	XP_011514488.1:n.2398+147C=
XM_011516185.2:c.2098+147C=	XP_011514487.1:n.2098+147C=
XM_011516186.3:c.2398+147C=	XP_011514488.1:n.2398+147C=
XM_017012195.1:c.2248+147C=	XP_016867684.1:n.2248+147C=
XM_017012196.1:c.2221+147C=	XP_016867685.1:n.2221+147C=
NM_000238.4:c.2398+147C= MANE Select	NP_000229.1:n.2398+147C=
NM_001204798.2:c.1525C=	NP_001191727.1:p.Pro509=
NM_172057.3:c.1378+147C=	NP_742054.1:n.1378+147C=