Canonical Allele Identifier: CA2685602034
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950148_150950149insGGGGGGCGGGGG , CM000669.2:g.150950148_150950149insGGGGGGCGGGGG GRCh38
NC_000007.13:g.150647236_150647237insGGGGGGCGGGGG , CM000669.1:g.150647236_150647237insGGGGGGCGGGGG GRCh37
NC_000007.12:g.150278169_150278170insGGGGGGCGGGGG NCBI36
NG_008916.1:g.32779_32780insCCCCGCCCCCCC , LRG_288:g.32779_32780insCCCCGCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000461280.2:n.1716_1717insCCCCGCCCCCCC
ENST00000684241.1:n.3231+20_3231+21insCCCCGCCCCCCC
ENST00000262186.10:c.2398+20_2398+21insCCCCGCCCCCCC MANE Select ENSP00000262186.5:n.2398+20_2398+21insCCCCGCCCCCCC
ENST00000330883.9:c.1378+20_1378+21insCCCCGCCCCCCC ENSP00000328531.4:n.1378+20_1378+21insCCCCGCCCCCCC
ENST00000262186.9:c.2398+20_2398+21insCCCCGCCCCCCC ENSP00000262186.5:n.2398+20_2398+21insCCCCGCCCCCCC
ENST00000330883.8:c.1378+20_1378+21insCCCCGCCCCCCC ENSP00000328531.4:n.1378+20_1378+21insCCCCGCCCCCCC
ENST00000430723.4:c.2070_2071insCCCCGCCCCCCC ENSP00000387657.4:p.Gly690_Thr691insProArgProPro
ENST00000461280.1:n.1705_1706insCCCCGCCCCCCC
ENST00000473610.5:n.2050_2051insCCCCGCCCCCCC
ENST00000532957.5:n.2641_2642insCCCCGCCCCCCC
NM_000238.3:c.2398+20_2398+21insCCCCGCCCCCCC , LRG_288t1:c.2398+20_2398+21insCCCCGCCCCCCC NP_000229.1:n.2398+20_2398+21insCCCCGCCCCCCC
NM_001204798.1:c.1398_1399insCCCCGCCCCCCC NP_001191727.1:p.Gly466_Thr467insProArgProPro
NM_172056.2:c.2418_2419insCCCCGCCCCCCC , LRG_288t2:c.2418_2419insCCCCGCCCCCCC NP_742053.1:p.Gly806_Thr807insProArgProPro
NM_172057.2:c.1378+20_1378+21insCCCCGCCCCCCC , LRG_288t3:c.1378+20_1378+21insCCCCGCCCCCCC NP_742054.1:n.1378+20_1378+21insCCCCGCCCCCCC
XM_011516185.1:c.2098+20_2098+21insCCCCGCCCCCCC XP_011514487.1:n.2098+20_2098+21insCCCCGCCCCCCC
XM_011516186.1:c.2398+20_2398+21insCCCCGCCCCCCC XP_011514488.1:n.2398+20_2398+21insCCCCGCCCCCCC
XM_011516185.2:c.2098+20_2098+21insCCCCGCCCCCCC XP_011514487.1:n.2098+20_2098+21insCCCCGCCCCCCC
XM_011516186.3:c.2398+20_2398+21insCCCCGCCCCCCC XP_011514488.1:n.2398+20_2398+21insCCCCGCCCCCCC
XM_017012195.1:c.2248+20_2248+21insCCCCGCCCCCCC XP_016867684.1:n.2248+20_2248+21insCCCCGCCCCCCC
XM_017012196.1:c.2221+20_2221+21insCCCCGCCCCCCC XP_016867685.1:n.2221+20_2221+21insCCCCGCCCCCCC
NM_000238.4:c.2398+20_2398+21insCCCCGCCCCCCC MANE Select NP_000229.1:n.2398+20_2398+21insCCCCGCCCCCCC
NM_001204798.2:c.1398_1399insCCCCGCCCCCCC NP_001191727.1:p.Gly466_Thr467insProArgProPro
NM_172057.3:c.1378+20_1378+21insCCCCGCCCCCCC NP_742054.1:n.1378+20_1378+21insCCCCGCCCCCCC