Canonical Allele Identifier: CA2685607604

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150951380-T-TCCAGGAAACC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951381_150951382insCAGGAAACCC , CM000669.2:g.150951381_150951382insCAGGAAACCC	GRCh38
NC_000007.13:g.150648469_150648470insCAGGAAACCC , CM000669.1:g.150648469_150648470insCAGGAAACCC	GRCh37
NC_000007.12:g.150279402_150279403insCAGGAAACCC	NCBI36
NG_008916.1:g.31546_31547insGGTTTCCTGG , LRG_288:g.31546_31547insGGTTTCCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1243+67_1243+68insGGTTTCCTGG
ENST00000683359.1:n.69+67_69+68insGGTTTCCTGG
ENST00000684241.1:n.2778+67_2778+68insGGTTTCCTGG
ENST00000262186.10:c.1945+67_1945+68insGGTTTCCTGG MANE Select	ENSP00000262186.5:n.1945+67_1945+68insGGTTTCCTGG
ENST00000330883.9:c.925+67_925+68insGGTTTCCTGG	ENSP00000328531.4:n.925+67_925+68insGGTTTCCTGG
ENST00000262186.9:c.1945+67_1945+68insGGTTTCCTGG	ENSP00000262186.5:n.1945+67_1945+68insGGTTTCCTGG
ENST00000330883.8:c.925+67_925+68insGGTTTCCTGG	ENSP00000328531.4:n.925+67_925+68insGGTTTCCTGG
ENST00000430723.4:c.1597+67_1597+68insGGTTTCCTGG	ENSP00000387657.4:n.1597+67_1597+68insGGTTTCCTGG
ENST00000461280.1:n.1232+67_1232+68insGGTTTCCTGG
ENST00000473610.5:n.1317_1318insGGTTTCCTGG
ENST00000532957.5:n.2168+67_2168+68insGGTTTCCTGG
NM_000238.3:c.1945+67_1945+68insGGTTTCCTGG , LRG_288t1:c.1945+67_1945+68insGGTTTCCTGG	NP_000229.1:n.1945+67_1945+68insGGTTTCCTGG
NM_001204798.1:c.925+67_925+68insGGTTTCCTGG	NP_001191727.1:n.925+67_925+68insGGTTTCCTGG
NM_172056.2:c.1945+67_1945+68insGGTTTCCTGG , LRG_288t2:c.1945+67_1945+68insGGTTTCCTGG	NP_742053.1:n.1945+67_1945+68insGGTTTCCTGG
NM_172057.2:c.925+67_925+68insGGTTTCCTGG , LRG_288t3:c.925+67_925+68insGGTTTCCTGG	NP_742054.1:n.925+67_925+68insGGTTTCCTGG
XM_011516185.1:c.1645+67_1645+68insGGTTTCCTGG	XP_011514487.1:n.1645+67_1645+68insGGTTTCCTGG
XM_011516186.1:c.1945+67_1945+68insGGTTTCCTGG	XP_011514488.1:n.1945+67_1945+68insGGTTTCCTGG
XM_011516185.2:c.1645+67_1645+68insGGTTTCCTGG	XP_011514487.1:n.1645+67_1645+68insGGTTTCCTGG
XM_011516186.3:c.1945+67_1945+68insGGTTTCCTGG	XP_011514488.1:n.1945+67_1945+68insGGTTTCCTGG
XM_017012195.1:c.1795+67_1795+68insGGTTTCCTGG	XP_016867684.1:n.1795+67_1795+68insGGTTTCCTGG
XM_017012196.1:c.1768+67_1768+68insGGTTTCCTGG	XP_016867685.1:n.1768+67_1768+68insGGTTTCCTGG
NM_000238.4:c.1945+67_1945+68insGGTTTCCTGG MANE Select	NP_000229.1:n.1945+67_1945+68insGGTTTCCTGG
NM_001204798.2:c.925+67_925+68insGGTTTCCTGG	NP_001191727.1:n.925+67_925+68insGGTTTCCTGG
NM_172057.3:c.925+67_925+68insGGTTTCCTGG	NP_742054.1:n.925+67_925+68insGGTTTCCTGG