Canonical Allele Identifier: CA2685601784

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150950028-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950031del , CM000669.2:g.150950031del	GRCh38
NC_000007.13:g.150647119del , CM000669.1:g.150647119del	GRCh37
NC_000007.12:g.150278052del	NCBI36
NG_008916.1:g.32898del , LRG_288:g.32898del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1835del
ENST00000684241.1:n.3231+139del
ENST00000262186.10:c.2398+139del MANE Select	ENSP00000262186.5:n.2398+139del
ENST00000330883.9:c.1378+139del	ENSP00000328531.4:n.1378+139del
ENST00000262186.9:c.2398+139del	ENSP00000262186.5:n.2398+139del
ENST00000330883.8:c.1378+139del	ENSP00000328531.4:n.1378+139del
ENST00000430723.4:c.2189del	ENSP00000387657.4:p.Asn730ThrfsTer?
ENST00000461280.1:n.1824del
ENST00000473610.5:n.2169del
ENST00000532957.5:n.2760del
NM_000238.3:c.2398+139del , LRG_288t1:c.2398+139del	NP_000229.1:n.2398+139del
NM_001204798.1:c.1517del	NP_001191727.1:p.Asn506ThrfsTer?
NM_172056.2:c.2537del , LRG_288t2:c.2537del	NP_742053.1:p.Asn846ThrfsTer?
NM_172057.2:c.1378+139del , LRG_288t3:c.1378+139del	NP_742054.1:n.1378+139del
XM_011516185.1:c.2098+139del	XP_011514487.1:n.2098+139del
XM_011516186.1:c.2398+139del	XP_011514488.1:n.2398+139del
XM_011516185.2:c.2098+139del	XP_011514487.1:n.2098+139del
XM_011516186.3:c.2398+139del	XP_011514488.1:n.2398+139del
XM_017012195.1:c.2248+139del	XP_016867684.1:n.2248+139del
XM_017012196.1:c.2221+139del	XP_016867685.1:n.2221+139del
NM_000238.4:c.2398+139del MANE Select	NP_000229.1:n.2398+139del
NM_001204798.2:c.1517del	NP_001191727.1:p.Asn506ThrfsTer?
NM_172057.3:c.1378+139del	NP_742054.1:n.1378+139del