Canonical Allele Identifier: CA2778425793

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950144_150950145insCGGGGGGGGGGGGGGGGGGGG , CM000669.2:g.150950144_150950145insCGGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000007.13:g.150647232_150647233insCGGGGGGGGGGGGGGGGGGGG , CM000669.1:g.150647232_150647233insCGGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000007.12:g.150278165_150278166insCGGGGGGGGGGGGGGGGGGGG	NCBI36
NG_008916.1:g.32782_32783insCCCCCCCCCCCCCCCCCCCCG , LRG_288:g.32782_32783insCCCCCCCCCCCCCCCCCCCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1719_1720insCCCCCCCCCCCCCCCCCCCCG
ENST00000684241.1:n.3231+23_3231+24insCCCCCCCCCCCCCCCCCCCCG
ENST00000262186.10:c.2398+23_2398+24insCCCCCCCCCCCCCCCCCCCCG MANE Select	ENSP00000262186.5:n.2398+23_2398+24insCCCCCCCCCCCCCCCCCCCCG
ENST00000330883.9:c.1378+23_1378+24insCCCCCCCCCCCCCCCCCCCCG	ENSP00000328531.4:n.1378+23_1378+24insCCCCCCCCCCCCCCCCCCCCG
ENST00000262186.9:c.2398+23_2398+24insCCCCCCCCCCCCCCCCCCCCG	ENSP00000262186.5:n.2398+23_2398+24insCCCCCCCCCCCCCCCCCCCCG
ENST00000330883.8:c.1378+23_1378+24insCCCCCCCCCCCCCCCCCCCCG	ENSP00000328531.4:n.1378+23_1378+24insCCCCCCCCCCCCCCCCCCCCG
ENST00000430723.4:c.2073_2074insCCCCCCCCCCCCCCCCCCCCG	ENSP00000387657.4:p.Thr691_Gly692insProProProProProProPro
ENST00000461280.1:n.1708_1709insCCCCCCCCCCCCCCCCCCCCG
ENST00000473610.5:n.2053_2054insCCCCCCCCCCCCCCCCCCCCG
ENST00000532957.5:n.2644_2645insCCCCCCCCCCCCCCCCCCCCG
NM_000238.3:c.2398+23_2398+24insCCCCCCCCCCCCCCCCCCCCG , LRG_288t1:c.2398+23_2398+24insCCCCCCCCCCCCCCCCCCCCG	NP_000229.1:n.2398+23_2398+24insCCCCCCCCCCCCCCCCCCCCG
NM_001204798.1:c.1401_1402insCCCCCCCCCCCCCCCCCCCCG	NP_001191727.1:p.Thr467_Gly468insProProProProProProPro
NM_172056.2:c.2421_2422insCCCCCCCCCCCCCCCCCCCCG , LRG_288t2:c.2421_2422insCCCCCCCCCCCCCCCCCCCCG	NP_742053.1:p.Thr807_Gly808insProProProProProProPro
NM_172057.2:c.1378+23_1378+24insCCCCCCCCCCCCCCCCCCCCG , LRG_288t3:c.1378+23_1378+24insCCCCCCCCCCCCCCCCCCCCG	NP_742054.1:n.1378+23_1378+24insCCCCCCCCCCCCCCCCCCCCG
XM_011516185.1:c.2098+23_2098+24insCCCCCCCCCCCCCCCCCCCCG	XP_011514487.1:n.2098+23_2098+24insCCCCCCCCCCCCCCCCCCCCG
XM_011516186.1:c.2398+23_2398+24insCCCCCCCCCCCCCCCCCCCCG	XP_011514488.1:n.2398+23_2398+24insCCCCCCCCCCCCCCCCCCCCG
XM_011516185.2:c.2098+23_2098+24insCCCCCCCCCCCCCCCCCCCCG	XP_011514487.1:n.2098+23_2098+24insCCCCCCCCCCCCCCCCCCCCG
XM_011516186.3:c.2398+23_2398+24insCCCCCCCCCCCCCCCCCCCCG	XP_011514488.1:n.2398+23_2398+24insCCCCCCCCCCCCCCCCCCCCG
XM_017012195.1:c.2248+23_2248+24insCCCCCCCCCCCCCCCCCCCCG	XP_016867684.1:n.2248+23_2248+24insCCCCCCCCCCCCCCCCCCCCG
XM_017012196.1:c.2221+23_2221+24insCCCCCCCCCCCCCCCCCCCCG	XP_016867685.1:n.2221+23_2221+24insCCCCCCCCCCCCCCCCCCCCG
NM_000238.4:c.2398+23_2398+24insCCCCCCCCCCCCCCCCCCCCG MANE Select	NP_000229.1:n.2398+23_2398+24insCCCCCCCCCCCCCCCCCCCCG
NM_001204798.2:c.1401_1402insCCCCCCCCCCCCCCCCCCCCG	NP_001191727.1:p.Thr467_Gly468insProProProProProProPro
NM_172057.3:c.1378+23_1378+24insCCCCCCCCCCCCCCCCCCCCG	NP_742054.1:n.1378+23_1378+24insCCCCCCCCCCCCCCCCCCCCG