Canonical Allele Identifier: CA1752420034

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150959681A= , CM000669.2:g.150959681A=	GRCh38
NC_000007.13:g.150656769A= , CM000669.1:g.150656769A=	GRCh37
NC_000007.12:g.150287702A=	NCBI36
NG_008916.1:g.23246T= , LRG_288:g.23246T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1196T=
ENST00000262186.10:c.363T= MANE Select	ENSP00000262186.5:p.Ala121=
ENST00000262186.9:c.363T=	ENSP00000262186.5:p.Ala121=
ENST00000430723.4:c.186T=	ENSP00000387657.4:p.Ala62=
ENST00000532957.5:n.586T=
NM_000238.3:c.363T= , LRG_288t1:c.363T=	NP_000229.1:p.Ala121=
NM_172056.2:c.363T= , LRG_288t2:c.363T=	NP_742053.1:p.Ala121=
XM_011516185.1:c.63T=	XP_011514487.1:p.Ala21=
XM_011516186.1:c.363T=	XP_011514488.1:p.Ala121=
XM_011516185.2:c.63T=	XP_011514487.1:p.Ala21=
XM_011516186.3:c.363T=	XP_011514488.1:p.Ala121=
XM_017012195.1:c.213T=	XP_016867684.1:p.Ala71=
XM_017012196.1:c.186T=	XP_016867685.1:p.Ala62=
NM_000238.4:c.363T= MANE Select	NP_000229.1:p.Ala121=