Canonical Allele Identifier: CA1752433488

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950277T= , CM000669.2:g.150950277T=	GRCh38
NC_000007.13:g.150647365T= , CM000669.1:g.150647365T=	GRCh37
NC_000007.12:g.150278298T=	NCBI36
NG_008916.1:g.32650A= , LRG_288:g.32650A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1587A=
ENST00000684241.1:n.3122A=
ENST00000262186.10:c.2289A= MANE Select	ENSP00000262186.5:p.Ala763=
ENST00000330883.9:c.1269A=	ENSP00000328531.4:p.Ala423=
ENST00000262186.9:c.2289A=	ENSP00000262186.5:p.Ala763=
ENST00000330883.8:c.1269A=	ENSP00000328531.4:p.Ala423=
ENST00000430723.4:c.1941A=	ENSP00000387657.4:p.Ala647=
ENST00000461280.1:n.1576A=
ENST00000473610.5:n.1921A=
ENST00000532957.5:n.2512A=
NM_000238.3:c.2289A= , LRG_288t1:c.2289A=	NP_000229.1:p.Ala763=
NM_001204798.1:c.1269A=	NP_001191727.1:p.Ala423=
NM_172056.2:c.2289A= , LRG_288t2:c.2289A=	NP_742053.1:p.Ala763=
NM_172057.2:c.1269A= , LRG_288t3:c.1269A=	NP_742054.1:p.Ala423=
XM_011516185.1:c.1989A=	XP_011514487.1:p.Ala663=
XM_011516186.1:c.2289A=	XP_011514488.1:p.Ala763=
XM_011516185.2:c.1989A=	XP_011514487.1:p.Ala663=
XM_011516186.3:c.2289A=	XP_011514488.1:p.Ala763=
XM_017012195.1:c.2139A=	XP_016867684.1:p.Ala713=
XM_017012196.1:c.2112A=	XP_016867685.1:p.Ala704=
NM_000238.4:c.2289A= MANE Select	NP_000229.1:p.Ala763=
NM_001204798.2:c.1269A=	NP_001191727.1:p.Ala423=
NM_172057.3:c.1269A=	NP_742054.1:p.Ala423=