Canonical Allele Identifier: CA1752434368

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951063G= , CM000669.2:g.150951063G=	GRCh38
NC_000007.13:g.150648151G= , CM000669.1:g.150648151G=	GRCh37
NC_000007.12:g.150279084G=	NCBI36
NG_008916.1:g.31864C= , LRG_288:g.31864C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1301C=
ENST00000683359.1:n.127C=
ENST00000684241.1:n.2836C=
ENST00000262186.10:c.2003C= MANE Select	ENSP00000262186.5:p.Ser668=
ENST00000330883.9:c.983C=	ENSP00000328531.4:p.Ser328=
ENST00000262186.9:c.2003C=	ENSP00000262186.5:p.Ser668=
ENST00000330883.8:c.983C=	ENSP00000328531.4:p.Ser328=
ENST00000430723.4:c.1655C=	ENSP00000387657.4:p.Ser552=
ENST00000461280.1:n.1290C=
ENST00000473610.5:n.1635C=
ENST00000532957.5:n.2226C=
NM_000238.3:c.2003C= , LRG_288t1:c.2003C=	NP_000229.1:p.Ser668=
NM_001204798.1:c.983C=	NP_001191727.1:p.Ser328=
NM_172056.2:c.2003C= , LRG_288t2:c.2003C=	NP_742053.1:p.Ser668=
NM_172057.2:c.983C= , LRG_288t3:c.983C=	NP_742054.1:p.Ser328=
XM_011516185.1:c.1703C=	XP_011514487.1:p.Ser568=
XM_011516186.1:c.2003C=	XP_011514488.1:p.Ser668=
XM_011516185.2:c.1703C=	XP_011514487.1:p.Ser568=
XM_011516186.3:c.2003C=	XP_011514488.1:p.Ser668=
XM_017012195.1:c.1853C=	XP_016867684.1:p.Ser618=
XM_017012196.1:c.1826C=	XP_016867685.1:p.Ser609=
NM_000238.4:c.2003C= MANE Select	NP_000229.1:p.Ser668=
NM_001204798.2:c.983C=	NP_001191727.1:p.Ser328=
NM_172057.3:c.983C=	NP_742054.1:p.Ser328=