Canonical Allele Identifier: CA2685607536

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150951333-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951334del , CM000669.2:g.150951334del	GRCh38
NC_000007.13:g.150648422del , CM000669.1:g.150648422del	GRCh37
NC_000007.12:g.150279355del	NCBI36
NG_008916.1:g.31593del , LRG_288:g.31593del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1243+114del
ENST00000683359.1:n.69+114del
ENST00000684241.1:n.2778+114del
ENST00000262186.10:c.1945+114del MANE Select	ENSP00000262186.5:n.1945+114del
ENST00000330883.9:c.925+114del	ENSP00000328531.4:n.925+114del
ENST00000262186.9:c.1945+114del	ENSP00000262186.5:n.1945+114del
ENST00000330883.8:c.925+114del	ENSP00000328531.4:n.925+114del
ENST00000430723.4:c.1597+114del	ENSP00000387657.4:n.1597+114del
ENST00000461280.1:n.1232+114del
ENST00000473610.5:n.1364del
ENST00000532957.5:n.2168+114del
NM_000238.3:c.1945+114del , LRG_288t1:c.1945+114del	NP_000229.1:n.1945+114del
NM_001204798.1:c.925+114del	NP_001191727.1:n.925+114del
NM_172056.2:c.1945+114del , LRG_288t2:c.1945+114del	NP_742053.1:n.1945+114del
NM_172057.2:c.925+114del , LRG_288t3:c.925+114del	NP_742054.1:n.925+114del
XM_011516185.1:c.1645+114del	XP_011514487.1:n.1645+114del
XM_011516186.1:c.1945+114del	XP_011514488.1:n.1945+114del
XM_011516185.2:c.1645+114del	XP_011514487.1:n.1645+114del
XM_011516186.3:c.1945+114del	XP_011514488.1:n.1945+114del
XM_017012195.1:c.1795+114del	XP_016867684.1:n.1795+114del
XM_017012196.1:c.1768+114del	XP_016867685.1:n.1768+114del
NM_000238.4:c.1945+114del MANE Select	NP_000229.1:n.1945+114del
NM_001204798.2:c.925+114del	NP_001191727.1:n.925+114del
NM_172057.3:c.925+114del	NP_742054.1:n.925+114del