Canonical Allele Identifier: CA1752431810

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150948859T= , CM000669.2:g.150948859T=	GRCh38
NC_000007.13:g.150645947T= , CM000669.1:g.150645947T=	GRCh37
NC_000007.12:g.150276880T=	NCBI36
NG_008916.1:g.34068A= , LRG_288:g.34068A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.3422A=
ENST00000262186.10:c.2589A= MANE Select	ENSP00000262186.5:p.Arg863=
ENST00000330883.9:c.1569A=	ENSP00000328531.4:p.Arg523=
ENST00000262186.9:c.2589A=	ENSP00000262186.5:p.Arg863=
ENST00000330883.8:c.1569A=	ENSP00000328531.4:p.Arg523=
NM_000238.3:c.2589A= , LRG_288t1:c.2589A=	NP_000229.1:p.Arg863=
NM_172057.2:c.1569A= , LRG_288t3:c.1569A=	NP_742054.1:p.Arg523=
XM_011516185.1:c.2289A=	XP_011514487.1:p.Arg763=
XM_011516186.1:c.2589A=	XP_011514488.1:p.Arg863=
XM_011516185.2:c.2289A=	XP_011514487.1:p.Arg763=
XM_011516186.3:c.2589A=	XP_011514488.1:p.Arg863=
XM_017012195.1:c.2439A=	XP_016867684.1:p.Arg813=
XM_017012196.1:c.2412A=	XP_016867685.1:p.Arg804=
NM_000238.4:c.2589A= MANE Select	NP_000229.1:p.Arg863=
NM_172057.3:c.1569A=	NP_742054.1:p.Arg523=