Canonical Allele Identifier: CA1752409999

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951582C= , CM000669.2:g.150951582C=	GRCh38
NC_000007.13:g.150648670C= , CM000669.1:g.150648670C=	GRCh37
NC_000007.12:g.150279603C=	NCBI36
NG_008916.1:g.31345G= , LRG_288:g.31345G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1109G=
ENST00000684241.1:n.2644G=
ENST00000262186.10:c.1811G= MANE Select	ENSP00000262186.5:p.Gly604=
ENST00000330883.9:c.791G=	ENSP00000328531.4:p.Gly264=
ENST00000262186.9:c.1811G=	ENSP00000262186.5:p.Gly604=
ENST00000330883.8:c.791G=	ENSP00000328531.4:p.Gly264=
ENST00000430723.4:c.1463G=	ENSP00000387657.4:p.Gly488=
ENST00000461280.1:n.1098G=
ENST00000473610.5:n.1116G=
ENST00000532957.5:n.2034G=
NM_000238.3:c.1811G= , LRG_288t1:c.1811G=	NP_000229.1:p.Gly604=
NM_001204798.1:c.791G=	NP_001191727.1:p.Gly264=
NM_172056.2:c.1811G= , LRG_288t2:c.1811G=	NP_742053.1:p.Gly604=
NM_172057.2:c.791G= , LRG_288t3:c.791G=	NP_742054.1:p.Gly264=
XM_011516185.1:c.1511G=	XP_011514487.1:p.Gly504=
XM_011516186.1:c.1811G=	XP_011514488.1:p.Gly604=
XM_011516185.2:c.1511G=	XP_011514487.1:p.Gly504=
XM_011516186.3:c.1811G=	XP_011514488.1:p.Gly604=
XM_017012195.1:c.1661G=	XP_016867684.1:p.Gly554=
XM_017012196.1:c.1634G=	XP_016867685.1:p.Gly545=
NM_000238.4:c.1811G= MANE Select	NP_000229.1:p.Gly604=
NM_001204798.2:c.791G=	NP_001191727.1:p.Gly264=
NM_172057.3:c.791G=	NP_742054.1:p.Gly264=