Canonical Allele Identifier: CA1752433619

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950348A= , CM000669.2:g.150950348A=	GRCh38
NC_000007.13:g.150647436A= , CM000669.1:g.150647436A=	GRCh37
NC_000007.12:g.150278369A=	NCBI36
NG_008916.1:g.32579T= , LRG_288:g.32579T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1516T=
ENST00000684241.1:n.3051T=
ENST00000262186.10:c.2218T= MANE Select	ENSP00000262186.5:p.Cys740=
ENST00000330883.9:c.1198T=	ENSP00000328531.4:p.Cys400=
ENST00000262186.9:c.2218T=	ENSP00000262186.5:p.Cys740=
ENST00000330883.8:c.1198T=	ENSP00000328531.4:p.Cys400=
ENST00000430723.4:c.1870T=	ENSP00000387657.4:p.Cys624=
ENST00000461280.1:n.1505T=
ENST00000473610.5:n.1850T=
ENST00000532957.5:n.2441T=
NM_000238.3:c.2218T= , LRG_288t1:c.2218T=	NP_000229.1:p.Cys740=
NM_001204798.1:c.1198T=	NP_001191727.1:p.Cys400=
NM_172056.2:c.2218T= , LRG_288t2:c.2218T=	NP_742053.1:p.Cys740=
NM_172057.2:c.1198T= , LRG_288t3:c.1198T=	NP_742054.1:p.Cys400=
XM_011516185.1:c.1918T=	XP_011514487.1:p.Cys640=
XM_011516186.1:c.2218T=	XP_011514488.1:p.Cys740=
XM_011516185.2:c.1918T=	XP_011514487.1:p.Cys640=
XM_011516186.3:c.2218T=	XP_011514488.1:p.Cys740=
XM_017012195.1:c.2068T=	XP_016867684.1:p.Cys690=
XM_017012196.1:c.2041T=	XP_016867685.1:p.Cys681=
NM_000238.4:c.2218T= MANE Select	NP_000229.1:p.Cys740=
NM_001204798.2:c.1198T=	NP_001191727.1:p.Cys400=
NM_172057.3:c.1198T=	NP_742054.1:p.Cys400=