Canonical Allele Identifier: CA2778425817

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950148_150950149insGGGGGGGGCGGGGGGGGGGG , CM000669.2:g.150950148_150950149insGGGGGGGGCGGGGGGGGGGG	GRCh38
NC_000007.13:g.150647236_150647237insGGGGGGGGCGGGGGGGGGGG , CM000669.1:g.150647236_150647237insGGGGGGGGCGGGGGGGGGGG	GRCh37
NC_000007.12:g.150278169_150278170insGGGGGGGGCGGGGGGGGGGG	NCBI36
NG_008916.1:g.32779_32780insCCCCCCCCCCGCCCCCCCCC , LRG_288:g.32779_32780insCCCCCCCCCCGCCCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1716_1717insCCCCCCCCCCGCCCCCCCCC
ENST00000684241.1:n.3231+20_3231+21insCCCCCCCCCCGCCCCCCCCC
ENST00000262186.10:c.2398+20_2398+21insCCCCCCCCCCGCCCCCCCCC MANE Select	ENSP00000262186.5:n.2398+20_2398+21insCCCCCCCCCCGCCCCCCCCC
ENST00000330883.9:c.1378+20_1378+21insCCCCCCCCCCGCCCCCCCCC	ENSP00000328531.4:n.1378+20_1378+21insCCCCCCCCCCGCCCCCCCCC
ENST00000262186.9:c.2398+20_2398+21insCCCCCCCCCCGCCCCCCCCC	ENSP00000262186.5:n.2398+20_2398+21insCCCCCCCCCCGCCCCCCCCC
ENST00000330883.8:c.1378+20_1378+21insCCCCCCCCCCGCCCCCCCCC	ENSP00000328531.4:n.1378+20_1378+21insCCCCCCCCCCGCCCCCCCCC
ENST00000430723.4:c.2070_2071insCCCCCCCCCCGCCCCCCCCC	ENSP00000387657.4:p.Thr691ProfsTer23
ENST00000461280.1:n.1705_1706insCCCCCCCCCCGCCCCCCCCC
ENST00000473610.5:n.2050_2051insCCCCCCCCCCGCCCCCCCCC
ENST00000532957.5:n.2641_2642insCCCCCCCCCCGCCCCCCCCC
NM_000238.3:c.2398+20_2398+21insCCCCCCCCCCGCCCCCCCCC , LRG_288t1:c.2398+20_2398+21insCCCCCCCCCCGCCCCCCCCC	NP_000229.1:n.2398+20_2398+21insCCCCCCCCCCGCCCCCCCCC
NM_001204798.1:c.1398_1399insCCCCCCCCCCGCCCCCCCCC	NP_001191727.1:p.Thr467ProfsTer23
NM_172056.2:c.2418_2419insCCCCCCCCCCGCCCCCCCCC , LRG_288t2:c.2418_2419insCCCCCCCCCCGCCCCCCCCC	NP_742053.1:p.Thr807ProfsTer23
NM_172057.2:c.1378+20_1378+21insCCCCCCCCCCGCCCCCCCCC , LRG_288t3:c.1378+20_1378+21insCCCCCCCCCCGCCCCCCCCC	NP_742054.1:n.1378+20_1378+21insCCCCCCCCCCGCCCCCCCCC
XM_011516185.1:c.2098+20_2098+21insCCCCCCCCCCGCCCCCCCCC	XP_011514487.1:n.2098+20_2098+21insCCCCCCCCCCGCCCCCCCCC
XM_011516186.1:c.2398+20_2398+21insCCCCCCCCCCGCCCCCCCCC	XP_011514488.1:n.2398+20_2398+21insCCCCCCCCCCGCCCCCCCCC
XM_011516185.2:c.2098+20_2098+21insCCCCCCCCCCGCCCCCCCCC	XP_011514487.1:n.2098+20_2098+21insCCCCCCCCCCGCCCCCCCCC
XM_011516186.3:c.2398+20_2398+21insCCCCCCCCCCGCCCCCCCCC	XP_011514488.1:n.2398+20_2398+21insCCCCCCCCCCGCCCCCCCCC
XM_017012195.1:c.2248+20_2248+21insCCCCCCCCCCGCCCCCCCCC	XP_016867684.1:n.2248+20_2248+21insCCCCCCCCCCGCCCCCCCCC
XM_017012196.1:c.2221+20_2221+21insCCCCCCCCCCGCCCCCCCCC	XP_016867685.1:n.2221+20_2221+21insCCCCCCCCCCGCCCCCCCCC
NM_000238.4:c.2398+20_2398+21insCCCCCCCCCCGCCCCCCCCC MANE Select	NP_000229.1:n.2398+20_2398+21insCCCCCCCCCCGCCCCCCCCC
NM_001204798.2:c.1398_1399insCCCCCCCCCCGCCCCCCCCC	NP_001191727.1:p.Thr467ProfsTer23
NM_172057.3:c.1378+20_1378+21insCCCCCCCCCCGCCCCCCCCC	NP_742054.1:n.1378+20_1378+21insCCCCCCCCCCGCCCCCCCCC