Canonical Allele Identifier: CA1752409888

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951566G= , CM000669.2:g.150951566G=	GRCh38
NC_000007.13:g.150648654G= , CM000669.1:g.150648654G=	GRCh37
NC_000007.12:g.150279587G=	NCBI36
NG_008916.1:g.31361C= , LRG_288:g.31361C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1125C=
ENST00000684241.1:n.2660C=
ENST00000262186.10:c.1827C= MANE Select	ENSP00000262186.5:p.Asp609=
ENST00000330883.9:c.807C=	ENSP00000328531.4:p.Asp269=
ENST00000262186.9:c.1827C=	ENSP00000262186.5:p.Asp609=
ENST00000330883.8:c.807C=	ENSP00000328531.4:p.Asp269=
ENST00000430723.4:c.1479C=	ENSP00000387657.4:p.Asp493=
ENST00000461280.1:n.1114C=
ENST00000473610.5:n.1132C=
ENST00000532957.5:n.2050C=
NM_000238.3:c.1827C= , LRG_288t1:c.1827C=	NP_000229.1:p.Asp609=
NM_001204798.1:c.807C=	NP_001191727.1:p.Asp269=
NM_172056.2:c.1827C= , LRG_288t2:c.1827C=	NP_742053.1:p.Asp609=
NM_172057.2:c.807C= , LRG_288t3:c.807C=	NP_742054.1:p.Asp269=
XM_011516185.1:c.1527C=	XP_011514487.1:p.Asp509=
XM_011516186.1:c.1827C=	XP_011514488.1:p.Asp609=
XM_011516185.2:c.1527C=	XP_011514487.1:p.Asp509=
XM_011516186.3:c.1827C=	XP_011514488.1:p.Asp609=
XM_017012195.1:c.1677C=	XP_016867684.1:p.Asp559=
XM_017012196.1:c.1650C=	XP_016867685.1:p.Asp550=
NM_000238.4:c.1827C= MANE Select	NP_000229.1:p.Asp609=
NM_001204798.2:c.807C=	NP_001191727.1:p.Asp269=
NM_172057.3:c.807C=	NP_742054.1:p.Asp269=