Canonical Allele Identifier: CA1752411783

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952567C= , CM000669.2:g.150952567C=	GRCh38
NC_000007.13:g.150649655C= , CM000669.1:g.150649655C=	GRCh37
NC_000007.12:g.150280588C=	NCBI36
NG_008916.1:g.30360G= , LRG_288:g.30360G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.713G=
ENST00000684116.1:n.308G=
ENST00000684241.1:n.2248G=
ENST00000262186.10:c.1415G= MANE Select	ENSP00000262186.5:p.Arg472=
ENST00000330883.9:c.395G=	ENSP00000328531.4:p.Arg132=
ENST00000262186.9:c.1415G=	ENSP00000262186.5:p.Arg472=
ENST00000330883.8:c.395G=	ENSP00000328531.4:p.Arg132=
ENST00000430723.4:c.1067G=	ENSP00000387657.4:p.Arg356=
ENST00000461280.1:n.702G=
ENST00000473610.5:n.720G=
ENST00000532957.5:n.1638G=
NM_000238.3:c.1415G= , LRG_288t1:c.1415G=	NP_000229.1:p.Arg472=
NM_001204798.1:c.395G=	NP_001191727.1:p.Arg132=
NM_172056.2:c.1415G= , LRG_288t2:c.1415G=	NP_742053.1:p.Arg472=
NM_172057.2:c.395G= , LRG_288t3:c.395G=	NP_742054.1:p.Arg132=
XM_011516185.1:c.1115G=	XP_011514487.1:p.Arg372=
XM_011516186.1:c.1415G=	XP_011514488.1:p.Arg472=
XM_011516185.2:c.1115G=	XP_011514487.1:p.Arg372=
XM_011516186.3:c.1415G=	XP_011514488.1:p.Arg472=
XM_017012195.1:c.1265G=	XP_016867684.1:p.Arg422=
XM_017012196.1:c.1238G=	XP_016867685.1:p.Arg413=
NM_000238.4:c.1415G= MANE Select	NP_000229.1:p.Arg472=
NM_001204798.2:c.395G=	NP_001191727.1:p.Arg132=
NM_172057.3:c.395G=	NP_742054.1:p.Arg132=