Canonical Allele Identifier: CA1752409786

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951550G= , CM000669.2:g.150951550G=	GRCh38
NC_000007.13:g.150648638G= , CM000669.1:g.150648638G=	GRCh37
NC_000007.12:g.150279571G=	NCBI36
NG_008916.1:g.31377C= , LRG_288:g.31377C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.1141C=
ENST00000684241.1:n.2676C=
ENST00000262186.10:c.1843C= MANE Select	ENSP00000262186.5:p.Leu615=
ENST00000330883.9:c.823C=	ENSP00000328531.4:p.Leu275=
ENST00000262186.9:c.1843C=	ENSP00000262186.5:p.Leu615=
ENST00000330883.8:c.823C=	ENSP00000328531.4:p.Leu275=
ENST00000430723.4:c.1495C=	ENSP00000387657.4:p.Leu499=
ENST00000461280.1:n.1130C=
ENST00000473610.5:n.1148C=
ENST00000532957.5:n.2066C=
NM_000238.3:c.1843C= , LRG_288t1:c.1843C=	NP_000229.1:p.Leu615=
NM_001204798.1:c.823C=	NP_001191727.1:p.Leu275=
NM_172056.2:c.1843C= , LRG_288t2:c.1843C=	NP_742053.1:p.Leu615=
NM_172057.2:c.823C= , LRG_288t3:c.823C=	NP_742054.1:p.Leu275=
XM_011516185.1:c.1543C=	XP_011514487.1:p.Leu515=
XM_011516186.1:c.1843C=	XP_011514488.1:p.Leu615=
XM_011516185.2:c.1543C=	XP_011514487.1:p.Leu515=
XM_011516186.3:c.1843C=	XP_011514488.1:p.Leu615=
XM_017012195.1:c.1693C=	XP_016867684.1:p.Leu565=
XM_017012196.1:c.1666C=	XP_016867685.1:p.Leu556=
NM_000238.4:c.1843C= MANE Select	NP_000229.1:p.Leu615=
NM_001204798.2:c.823C=	NP_001191727.1:p.Leu275=
NM_172057.3:c.823C=	NP_742054.1:p.Leu275=