Canonical Allele Identifier: CA1752412441

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952875G= , CM000669.2:g.150952875G=	GRCh38
NC_000007.13:g.150649963G= , CM000669.1:g.150649963G=	GRCh37
NC_000007.12:g.150280896G=	NCBI36
NG_008916.1:g.30052C= , LRG_288:g.30052C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.427-22C=
ENST00000684241.1:n.1962-22C=
ENST00000262186.10:c.1129-22C= MANE Select	ENSP00000262186.5:n.1129-22C=
ENST00000330883.9:c.109-22C=	ENSP00000328531.4:n.109-22C=
ENST00000262186.9:c.1129-22C=	ENSP00000262186.5:n.1129-22C=
ENST00000330883.8:c.109-22C=	ENSP00000328531.4:n.109-22C=
ENST00000430723.4:c.781-22C=	ENSP00000387657.4:n.781-22C=
ENST00000461280.1:n.416-22C=
ENST00000473610.5:n.434-22C=
ENST00000532957.5:n.1352-22C=
NM_000238.3:c.1129-22C= , LRG_288t1:c.1129-22C=	NP_000229.1:n.1129-22C=
NM_001204798.1:c.109-22C=	NP_001191727.1:n.109-22C=
NM_172056.2:c.1129-22C= , LRG_288t2:c.1129-22C=	NP_742053.1:n.1129-22C=
NM_172057.2:c.109-22C= , LRG_288t3:c.109-22C=	NP_742054.1:n.109-22C=
XM_011516185.1:c.829-22C=	XP_011514487.1:n.829-22C=
XM_011516186.1:c.1129-22C=	XP_011514488.1:n.1129-22C=
XM_011516185.2:c.829-22C=	XP_011514487.1:n.829-22C=
XM_011516186.3:c.1129-22C=	XP_011514488.1:n.1129-22C=
XM_017012195.1:c.979-22C=	XP_016867684.1:n.979-22C=
XM_017012196.1:c.952-22C=	XP_016867685.1:n.952-22C=
NM_000238.4:c.1129-22C= MANE Select	NP_000229.1:n.1129-22C=
NM_001204798.2:c.109-22C=	NP_001191727.1:n.109-22C=
NM_172057.3:c.109-22C=	NP_742054.1:n.109-22C=