Canonical Allele Identifier: CA2685601915

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150950145-A-AGGGGGGGGGGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950146_150950147insGGGGGGGGGGGGGGGGGGGGG , CM000669.2:g.150950146_150950147insGGGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000007.13:g.150647234_150647235insGGGGGGGGGGGGGGGGGGGGG , CM000669.1:g.150647234_150647235insGGGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000007.12:g.150278167_150278168insGGGGGGGGGGGGGGGGGGGGG	NCBI36
NG_008916.1:g.32781_32782insCCCCCCCCCCCCCCCCCCCCC , LRG_288:g.32781_32782insCCCCCCCCCCCCCCCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1718_1719insCCCCCCCCCCCCCCCCCCCCC
ENST00000684241.1:n.3231+22_3231+23insCCCCCCCCCCCCCCCCCCCCC
ENST00000262186.10:c.2398+22_2398+23insCCCCCCCCCCCCCCCCCCCCC MANE Select	ENSP00000262186.5:n.2398+22_2398+23insCCCCCCCCCCCCCCCCCCCCC
ENST00000330883.9:c.1378+22_1378+23insCCCCCCCCCCCCCCCCCCCCC	ENSP00000328531.4:n.1378+22_1378+23insCCCCCCCCCCCCCCCCCCCCC
ENST00000262186.9:c.2398+22_2398+23insCCCCCCCCCCCCCCCCCCCCC	ENSP00000262186.5:n.2398+22_2398+23insCCCCCCCCCCCCCCCCCCCCC
ENST00000330883.8:c.1378+22_1378+23insCCCCCCCCCCCCCCCCCCCCC	ENSP00000328531.4:n.1378+22_1378+23insCCCCCCCCCCCCCCCCCCCCC
ENST00000430723.4:c.2072_2073insCCCCCCCCCCCCCCCCCCCCC	ENSP00000387657.4:p.Thr691_Gly692insProProProProProProPro
ENST00000461280.1:n.1707_1708insCCCCCCCCCCCCCCCCCCCCC
ENST00000473610.5:n.2052_2053insCCCCCCCCCCCCCCCCCCCCC
ENST00000532957.5:n.2643_2644insCCCCCCCCCCCCCCCCCCCCC
NM_000238.3:c.2398+22_2398+23insCCCCCCCCCCCCCCCCCCCCC , LRG_288t1:c.2398+22_2398+23insCCCCCCCCCCCCCCCCCCCCC	NP_000229.1:n.2398+22_2398+23insCCCCCCCCCCCCCCCCCCCCC
NM_001204798.1:c.1400_1401insCCCCCCCCCCCCCCCCCCCCC	NP_001191727.1:p.Thr467_Gly468insProProProProProProPro
NM_172056.2:c.2420_2421insCCCCCCCCCCCCCCCCCCCCC , LRG_288t2:c.2420_2421insCCCCCCCCCCCCCCCCCCCCC	NP_742053.1:p.Thr807_Gly808insProProProProProProPro
NM_172057.2:c.1378+22_1378+23insCCCCCCCCCCCCCCCCCCCCC , LRG_288t3:c.1378+22_1378+23insCCCCCCCCCCCCCCCCCCCCC	NP_742054.1:n.1378+22_1378+23insCCCCCCCCCCCCCCCCCCCCC
XM_011516185.1:c.2098+22_2098+23insCCCCCCCCCCCCCCCCCCCCC	XP_011514487.1:n.2098+22_2098+23insCCCCCCCCCCCCCCCCCCCCC
XM_011516186.1:c.2398+22_2398+23insCCCCCCCCCCCCCCCCCCCCC	XP_011514488.1:n.2398+22_2398+23insCCCCCCCCCCCCCCCCCCCCC
XM_011516185.2:c.2098+22_2098+23insCCCCCCCCCCCCCCCCCCCCC	XP_011514487.1:n.2098+22_2098+23insCCCCCCCCCCCCCCCCCCCCC
XM_011516186.3:c.2398+22_2398+23insCCCCCCCCCCCCCCCCCCCCC	XP_011514488.1:n.2398+22_2398+23insCCCCCCCCCCCCCCCCCCCCC
XM_017012195.1:c.2248+22_2248+23insCCCCCCCCCCCCCCCCCCCCC	XP_016867684.1:n.2248+22_2248+23insCCCCCCCCCCCCCCCCCCCCC
XM_017012196.1:c.2221+22_2221+23insCCCCCCCCCCCCCCCCCCCCC	XP_016867685.1:n.2221+22_2221+23insCCCCCCCCCCCCCCCCCCCCC
NM_000238.4:c.2398+22_2398+23insCCCCCCCCCCCCCCCCCCCCC MANE Select	NP_000229.1:n.2398+22_2398+23insCCCCCCCCCCCCCCCCCCCCC
NM_001204798.2:c.1400_1401insCCCCCCCCCCCCCCCCCCCCC	NP_001191727.1:p.Thr467_Gly468insProProProProProProPro
NM_172057.3:c.1378+22_1378+23insCCCCCCCCCCCCCCCCCCCCC	NP_742054.1:n.1378+22_1378+23insCCCCCCCCCCCCCCCCCCCCC