Canonical Allele Identifier: CA369858884

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951730A>G , CM000669.2:g.150951730A>G	GRCh38
NC_000007.13:g.150648818A>G , CM000669.1:g.150648818A>G	GRCh37
NC_000007.12:g.150279751A>G	NCBI36
NG_008916.1:g.31197T>C , LRG_288:g.31197T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000238.4:c.1663T>C MANE Select	NP_000229.1:p.Cys555Arg
ENST00000262186.10:c.1663T>C MANE Select	ENSP00000262186.5:p.Cys555Arg
NM_000238.3:c.1663T>C , LRG_288t1:c.1663T>C	NP_000229.1:p.Cys555Arg
NM_001204798.1:c.643T>C	NP_001191727.1:p.Cys215Arg
NM_001204798.2:c.643T>C	NP_001191727.1:p.Cys215Arg
NM_172056.2:c.1663T>C , LRG_288t2:c.1663T>C	NP_742053.1:p.Cys555Arg
NM_172057.2:c.643T>C , LRG_288t3:c.643T>C	NP_742054.1:p.Cys215Arg
NM_172057.3:c.643T>C	NP_742054.1:p.Cys215Arg
ENST00000262186.9:c.1663T>C	ENSP00000262186.5:p.Cys555Arg
ENST00000330883.8:c.643T>C	ENSP00000328531.4:p.Cys215Arg
ENST00000330883.9:c.643T>C	ENSP00000328531.4:p.Cys215Arg
ENST00000430723.4:c.1315T>C	ENSP00000387657.4:p.Cys439Arg
ENST00000461280.1:n.950T>C
ENST00000461280.2:n.961T>C
ENST00000473610.5:n.968T>C
ENST00000532957.5:n.1886T>C
ENST00000684116.1:n.556T>C
ENST00000684241.1:n.2496T>C
XM_011516185.1:c.1363T>C	XP_011514487.1:p.Cys455Arg
XM_011516185.2:c.1363T>C	XP_011514487.1:p.Cys455Arg
XM_011516186.1:c.1663T>C	XP_011514488.1:p.Cys555Arg
XM_011516186.3:c.1663T>C	XP_011514488.1:p.Cys555Arg
XM_017012195.1:c.1513T>C	XP_016867684.1:p.Cys505Arg
XM_017012196.1:c.1486T>C	XP_016867685.1:p.Cys496Arg