Canonical Allele Identifier: CA1752418094

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958207G= , CM000669.2:g.150958207G=	GRCh38
NC_000007.13:g.150655295G= , CM000669.1:g.150655295G=	GRCh37
NC_000007.12:g.150286228G=	NCBI36
NG_008916.1:g.24720C= , LRG_288:g.24720C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1601C=
ENST00000262186.10:c.768C= MANE Select	ENSP00000262186.5:p.Leu256=
ENST00000262186.9:c.768C=	ENSP00000262186.5:p.Leu256=
ENST00000430723.4:c.420C=	ENSP00000387657.4:p.Leu140=
ENST00000532957.5:n.991C=
NM_000238.3:c.768C= , LRG_288t1:c.768C=	NP_000229.1:p.Leu256=
NM_172056.2:c.768C= , LRG_288t2:c.768C=	NP_742053.1:p.Leu256=
XM_011516185.1:c.468C=	XP_011514487.1:p.Leu156=
XM_011516186.1:c.768C=	XP_011514488.1:p.Leu256=
XM_011516185.2:c.468C=	XP_011514487.1:p.Leu156=
XM_011516186.3:c.768C=	XP_011514488.1:p.Leu256=
XM_017012195.1:c.618C=	XP_016867684.1:p.Leu206=
XM_017012196.1:c.591C=	XP_016867685.1:p.Leu197=
NM_000238.4:c.768C= MANE Select	NP_000229.1:p.Leu256=