Canonical Allele Identifier: CA1752434482

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951110A= , CM000669.2:g.150951110A=	GRCh38
NC_000007.13:g.150648198A= , CM000669.1:g.150648198A=	GRCh37
NC_000007.12:g.150279131A=	NCBI36
NG_008916.1:g.31817T= , LRG_288:g.31817T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1254T=
ENST00000683359.1:n.80T=
ENST00000684241.1:n.2789T=
ENST00000262186.10:c.1956T= MANE Select	ENSP00000262186.5:p.Tyr652=
ENST00000330883.9:c.936T=	ENSP00000328531.4:p.Tyr312=
ENST00000262186.9:c.1956T=	ENSP00000262186.5:p.Tyr652=
ENST00000330883.8:c.936T=	ENSP00000328531.4:p.Tyr312=
ENST00000430723.4:c.1608T=	ENSP00000387657.4:p.Tyr536=
ENST00000461280.1:n.1243T=
ENST00000473610.5:n.1588T=
ENST00000532957.5:n.2179T=
NM_000238.3:c.1956T= , LRG_288t1:c.1956T=	NP_000229.1:p.Tyr652=
NM_001204798.1:c.936T=	NP_001191727.1:p.Tyr312=
NM_172056.2:c.1956T= , LRG_288t2:c.1956T=	NP_742053.1:p.Tyr652=
NM_172057.2:c.936T= , LRG_288t3:c.936T=	NP_742054.1:p.Tyr312=
XM_011516185.1:c.1656T=	XP_011514487.1:p.Tyr552=
XM_011516186.1:c.1956T=	XP_011514488.1:p.Tyr652=
XM_011516185.2:c.1656T=	XP_011514487.1:p.Tyr552=
XM_011516186.3:c.1956T=	XP_011514488.1:p.Tyr652=
XM_017012195.1:c.1806T=	XP_016867684.1:p.Tyr602=
XM_017012196.1:c.1779T=	XP_016867685.1:p.Tyr593=
NM_000238.4:c.1956T= MANE Select	NP_000229.1:p.Tyr652=
NM_001204798.2:c.936T=	NP_001191727.1:p.Tyr312=
NM_172057.3:c.936T=	NP_742054.1:p.Tyr312=