Canonical Allele Identifier: CA1752417965

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958152T= , CM000669.2:g.150958152T=	GRCh38
NC_000007.13:g.150655240T= , CM000669.1:g.150655240T=	GRCh37
NC_000007.12:g.150286173T=	NCBI36
NG_008916.1:g.24775A= , LRG_288:g.24775A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684241.1:n.1656A=
ENST00000262186.10:c.823A= MANE Select	ENSP00000262186.5:p.Ser275=
ENST00000262186.9:c.823A=	ENSP00000262186.5:p.Ser275=
ENST00000430723.4:c.475A=	ENSP00000387657.4:p.Ser159=
ENST00000532957.5:n.1046A=
NM_000238.3:c.823A= , LRG_288t1:c.823A=	NP_000229.1:p.Ser275=
NM_172056.2:c.823A= , LRG_288t2:c.823A=	NP_742053.1:p.Ser275=
XM_011516185.1:c.523A=	XP_011514487.1:p.Ser175=
XM_011516186.1:c.823A=	XP_011514488.1:p.Ser275=
XM_011516185.2:c.523A=	XP_011514487.1:p.Ser175=
XM_011516186.3:c.823A=	XP_011514488.1:p.Ser275=
XM_017012195.1:c.673A=	XP_016867684.1:p.Ser225=
XM_017012196.1:c.646A=	XP_016867685.1:p.Ser216=
NM_000238.4:c.823A= MANE Select	NP_000229.1:p.Ser275=