Canonical Allele Identifier: CA2967120567

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950132dup , CM000669.2:g.150950132dup	GRCh38
NC_000007.13:g.150647220dup , CM000669.1:g.150647220dup	GRCh37
NC_000007.12:g.150278153dup	NCBI36
NG_008916.1:g.32797dup , LRG_288:g.32797dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1734dup
ENST00000684241.1:n.3231+38dup
ENST00000262186.10:c.2398+38dup MANE Select	ENSP00000262186.5:n.2398+38dup
ENST00000330883.9:c.1378+38dup	ENSP00000328531.4:n.1378+38dup
ENST00000262186.9:c.2398+38dup	ENSP00000262186.5:n.2398+38dup
ENST00000330883.8:c.1378+38dup	ENSP00000328531.4:n.1378+38dup
ENST00000430723.4:c.2088dup	ENSP00000387657.4:p.Ser697LeufsTer?
ENST00000461280.1:n.1723dup
ENST00000473610.5:n.2068dup
ENST00000532957.5:n.2659dup
NM_000238.3:c.2398+38dup , LRG_288t1:c.2398+38dup	NP_000229.1:n.2398+38dup
NM_001204798.1:c.1416dup	NP_001191727.1:p.Ser473LeufsTer?
NM_172056.2:c.2436dup , LRG_288t2:c.2436dup	NP_742053.1:p.Ser813LeufsTer?
NM_172057.2:c.1378+38dup , LRG_288t3:c.1378+38dup	NP_742054.1:n.1378+38dup
XM_011516185.1:c.2098+38dup	XP_011514487.1:n.2098+38dup
XM_011516186.1:c.2398+38dup	XP_011514488.1:n.2398+38dup
XM_011516185.2:c.2098+38dup	XP_011514487.1:n.2098+38dup
XM_011516186.3:c.2398+38dup	XP_011514488.1:n.2398+38dup
XM_017012195.1:c.2248+38dup	XP_016867684.1:n.2248+38dup
XM_017012196.1:c.2221+38dup	XP_016867685.1:n.2221+38dup
NM_000238.4:c.2398+38dup MANE Select	NP_000229.1:n.2398+38dup
NM_001204798.2:c.1416dup	NP_001191727.1:p.Ser473LeufsTer?
NM_172057.3:c.1378+38dup	NP_742054.1:n.1378+38dup