Canonical Allele Identifier: CA1752416953

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150957478C= , CM000669.2:g.150957478C=	GRCh38
NC_000007.13:g.150654566C= , CM000669.1:g.150654566C=	GRCh37
NC_000007.12:g.150285499C=	NCBI36
NG_008916.1:g.25449G= , LRG_288:g.25449G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1774G=
ENST00000262186.10:c.941G= MANE Select	ENSP00000262186.5:p.Gly314=
ENST00000262186.9:c.941G=	ENSP00000262186.5:p.Gly314=
ENST00000430723.4:c.593G=	ENSP00000387657.4:p.Gly198=
ENST00000532957.5:n.1164G=
NM_000238.3:c.941G= , LRG_288t1:c.941G=	NP_000229.1:p.Gly314=
NM_172056.2:c.941G= , LRG_288t2:c.941G=	NP_742053.1:p.Gly314=
XM_011516185.1:c.641G=	XP_011514487.1:p.Gly214=
XM_011516186.1:c.941G=	XP_011514488.1:p.Gly314=
XM_011516185.2:c.641G=	XP_011514487.1:p.Gly214=
XM_011516186.3:c.941G=	XP_011514488.1:p.Gly314=
XM_017012195.1:c.791G=	XP_016867684.1:p.Gly264=
XM_017012196.1:c.764G=	XP_016867685.1:p.Gly255=
NM_000238.4:c.941G= MANE Select	NP_000229.1:p.Gly314=