Canonical Allele Identifier: CA1752434064

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950883C= , CM000669.2:g.150950883C=	GRCh38
NC_000007.13:g.150647971C= , CM000669.1:g.150647971C=	GRCh37
NC_000007.12:g.150278904C=	NCBI36
NG_008916.1:g.32044G= , LRG_288:g.32044G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.1443+38G=
ENST00000683359.1:n.307G=
ENST00000684241.1:n.2978+38G=
ENST00000262186.10:c.2145+38G= MANE Select	ENSP00000262186.5:n.2145+38G=
ENST00000330883.9:c.1125+38G=	ENSP00000328531.4:n.1125+38G=
ENST00000262186.9:c.2145+38G=	ENSP00000262186.5:n.2145+38G=
ENST00000330883.8:c.1125+38G=	ENSP00000328531.4:n.1125+38G=
ENST00000430723.4:c.1797+38G=	ENSP00000387657.4:n.1797+38G=
ENST00000461280.1:n.1432+38G=
ENST00000473610.5:n.1777+38G=
ENST00000532957.5:n.2368+38G=
NM_000238.3:c.2145+38G= , LRG_288t1:c.2145+38G=	NP_000229.1:n.2145+38G=
NM_001204798.1:c.1125+38G=	NP_001191727.1:n.1125+38G=
NM_172056.2:c.2145+38G= , LRG_288t2:c.2145+38G=	NP_742053.1:n.2145+38G=
NM_172057.2:c.1125+38G= , LRG_288t3:c.1125+38G=	NP_742054.1:n.1125+38G=
XM_011516185.1:c.1845+38G=	XP_011514487.1:n.1845+38G=
XM_011516186.1:c.2145+38G=	XP_011514488.1:n.2145+38G=
XM_011516185.2:c.1845+38G=	XP_011514487.1:n.1845+38G=
XM_011516186.3:c.2145+38G=	XP_011514488.1:n.2145+38G=
XM_017012195.1:c.1995+38G=	XP_016867684.1:n.1995+38G=
XM_017012196.1:c.1968+38G=	XP_016867685.1:n.1968+38G=
NM_000238.4:c.2145+38G= MANE Select	NP_000229.1:n.2145+38G=
NM_001204798.2:c.1125+38G=	NP_001191727.1:n.1125+38G=
NM_172057.3:c.1125+38G=	NP_742054.1:n.1125+38G=