Canonical Allele Identifier: CA1752433382

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950206A= , CM000669.2:g.150950206A=	GRCh38
NC_000007.13:g.150647294A= , CM000669.1:g.150647294A=	GRCh37
NC_000007.12:g.150278227A=	NCBI36
NG_008916.1:g.32721T= , LRG_288:g.32721T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1658T=
ENST00000684241.1:n.3193T=
ENST00000262186.10:c.2360T= MANE Select	ENSP00000262186.5:p.Ile787=
ENST00000330883.9:c.1340T=	ENSP00000328531.4:p.Ile447=
ENST00000262186.9:c.2360T=	ENSP00000262186.5:p.Ile787=
ENST00000330883.8:c.1340T=	ENSP00000328531.4:p.Ile447=
ENST00000430723.4:c.2012T=	ENSP00000387657.4:p.Ile671=
ENST00000461280.1:n.1647T=
ENST00000473610.5:n.1992T=
ENST00000532957.5:n.2583T=
NM_000238.3:c.2360T= , LRG_288t1:c.2360T=	NP_000229.1:p.Ile787=
NM_001204798.1:c.1340T=	NP_001191727.1:p.Ile447=
NM_172056.2:c.2360T= , LRG_288t2:c.2360T=	NP_742053.1:p.Ile787=
NM_172057.2:c.1340T= , LRG_288t3:c.1340T=	NP_742054.1:p.Ile447=
XM_011516185.1:c.2060T=	XP_011514487.1:p.Ile687=
XM_011516186.1:c.2360T=	XP_011514488.1:p.Ile787=
XM_011516185.2:c.2060T=	XP_011514487.1:p.Ile687=
XM_011516186.3:c.2360T=	XP_011514488.1:p.Ile787=
XM_017012195.1:c.2210T=	XP_016867684.1:p.Ile737=
XM_017012196.1:c.2183T=	XP_016867685.1:p.Ile728=
NM_000238.4:c.2360T= MANE Select	NP_000229.1:p.Ile787=
NM_001204798.2:c.1340T=	NP_001191727.1:p.Ile447=
NM_172057.3:c.1340T=	NP_742054.1:p.Ile447=