Canonical Allele Identifier: CA1752419819

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959589G= , CM000669.2:g.150959589G=	GRCh38
NC_000007.13:g.150656677G= , CM000669.1:g.150656677G=	GRCh37
NC_000007.12:g.150287610G=	NCBI36
NG_008916.1:g.23338C= , LRG_288:g.23338C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1288C=
ENST00000262186.10:c.455C= MANE Select	ENSP00000262186.5:p.Thr152=
ENST00000262186.9:c.455C=	ENSP00000262186.5:p.Thr152=
ENST00000430723.4:c.234+44C=	ENSP00000387657.4:n.234+44C=
ENST00000532957.5:n.678C=
NM_000238.3:c.455C= , LRG_288t1:c.455C=	NP_000229.1:p.Thr152=
NM_172056.2:c.455C= , LRG_288t2:c.455C=	NP_742053.1:p.Thr152=
XM_011516185.1:c.155C=	XP_011514487.1:p.Thr52=
XM_011516186.1:c.455C=	XP_011514488.1:p.Thr152=
XM_011516185.2:c.155C=	XP_011514487.1:p.Thr52=
XM_011516186.3:c.455C=	XP_011514488.1:p.Thr152=
XM_017012195.1:c.305C=	XP_016867684.1:p.Thr102=
XM_017012196.1:c.278C=	XP_016867685.1:p.Thr93=
NM_000238.4:c.455C= MANE Select	NP_000229.1:p.Thr152=