Canonical Allele Identifier: CA1752411788

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952568G= , CM000669.2:g.150952568G=	GRCh38
NC_000007.13:g.150649656G= , CM000669.1:g.150649656G=	GRCh37
NC_000007.12:g.150280589G=	NCBI36
NG_008916.1:g.30359C= , LRG_288:g.30359C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.712C=
ENST00000684116.1:n.307C=
ENST00000684241.1:n.2247C=
ENST00000262186.10:c.1414C= MANE Select	ENSP00000262186.5:p.Arg472=
ENST00000330883.9:c.394C=	ENSP00000328531.4:p.Arg132=
ENST00000262186.9:c.1414C=	ENSP00000262186.5:p.Arg472=
ENST00000330883.8:c.394C=	ENSP00000328531.4:p.Arg132=
ENST00000430723.4:c.1066C=	ENSP00000387657.4:p.Arg356=
ENST00000461280.1:n.701C=
ENST00000473610.5:n.719C=
ENST00000532957.5:n.1637C=
NM_000238.3:c.1414C= , LRG_288t1:c.1414C=	NP_000229.1:p.Arg472=
NM_001204798.1:c.394C=	NP_001191727.1:p.Arg132=
NM_172056.2:c.1414C= , LRG_288t2:c.1414C=	NP_742053.1:p.Arg472=
NM_172057.2:c.394C= , LRG_288t3:c.394C=	NP_742054.1:p.Arg132=
XM_011516185.1:c.1114C=	XP_011514487.1:p.Arg372=
XM_011516186.1:c.1414C=	XP_011514488.1:p.Arg472=
XM_011516185.2:c.1114C=	XP_011514487.1:p.Arg372=
XM_011516186.3:c.1414C=	XP_011514488.1:p.Arg472=
XM_017012195.1:c.1264C=	XP_016867684.1:p.Arg422=
XM_017012196.1:c.1237C=	XP_016867685.1:p.Arg413=
NM_000238.4:c.1414C= MANE Select	NP_000229.1:p.Arg472=
NM_001204798.2:c.394C=	NP_001191727.1:p.Arg132=
NM_172057.3:c.394C=	NP_742054.1:p.Arg132=