Canonical Allele Identifier: CA2695208708

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950412del , CM000669.2:g.150950412del	GRCh38
NC_000007.13:g.150647500del , CM000669.1:g.150647500del	GRCh37
NC_000007.12:g.150278433del	NCBI36
NG_008916.1:g.32517del , LRG_288:g.32517del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1454del
ENST00000684241.1:n.2989del
ENST00000262186.10:c.2156del MANE Select	ENSP00000262186.5:p.Gly719AlafsTer14
ENST00000330883.9:c.1136del	ENSP00000328531.4:p.Gly379AlafsTer14
ENST00000262186.9:c.2156del	ENSP00000262186.5:p.Gly719AlafsTer14
ENST00000330883.8:c.1136del	ENSP00000328531.4:p.Gly379AlafsTer14
ENST00000430723.4:c.1808del	ENSP00000387657.4:p.Gly603AlafsTer14
ENST00000461280.1:n.1443del
ENST00000473610.5:n.1788del
ENST00000532957.5:n.2379del
NM_000238.3:c.2156del , LRG_288t1:c.2156del	NP_000229.1:p.Gly719AlafsTer14
NM_001204798.1:c.1136del	NP_001191727.1:p.Gly379AlafsTer14
NM_172056.2:c.2156del , LRG_288t2:c.2156del	NP_742053.1:p.Gly719AlafsTer14
NM_172057.2:c.1136del , LRG_288t3:c.1136del	NP_742054.1:p.Gly379AlafsTer14
XM_011516185.1:c.1856del	XP_011514487.1:p.Gly619AlafsTer14
XM_011516186.1:c.2156del	XP_011514488.1:p.Gly719AlafsTer14
XM_011516185.2:c.1856del	XP_011514487.1:p.Gly619AlafsTer14
XM_011516186.3:c.2156del	XP_011514488.1:p.Gly719AlafsTer14
XM_017012195.1:c.2006del	XP_016867684.1:p.Gly669AlafsTer14
XM_017012196.1:c.1979del	XP_016867685.1:p.Gly660AlafsTer14
NM_000238.4:c.2156del MANE Select	NP_000229.1:p.Gly719AlafsTer14
NM_001204798.2:c.1136del	NP_001191727.1:p.Gly379AlafsTer14
NM_172057.3:c.1136del	NP_742054.1:p.Gly379AlafsTer14