Canonical Allele Identifier: CA1752434418

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951093T= , CM000669.2:g.150951093T=	GRCh38
NC_000007.13:g.150648181T= , CM000669.1:g.150648181T=	GRCh37
NC_000007.12:g.150279114T=	NCBI36
NG_008916.1:g.31834A= , LRG_288:g.31834A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1271A=
ENST00000683359.1:n.97A=
ENST00000684241.1:n.2806A=
ENST00000262186.10:c.1973A= MANE Select	ENSP00000262186.5:p.Asn658=
ENST00000330883.9:c.953A=	ENSP00000328531.4:p.Asn318=
ENST00000262186.9:c.1973A=	ENSP00000262186.5:p.Asn658=
ENST00000330883.8:c.953A=	ENSP00000328531.4:p.Asn318=
ENST00000430723.4:c.1625A=	ENSP00000387657.4:p.Asn542=
ENST00000461280.1:n.1260A=
ENST00000473610.5:n.1605A=
ENST00000532957.5:n.2196A=
NM_000238.3:c.1973A= , LRG_288t1:c.1973A=	NP_000229.1:p.Asn658=
NM_001204798.1:c.953A=	NP_001191727.1:p.Asn318=
NM_172056.2:c.1973A= , LRG_288t2:c.1973A=	NP_742053.1:p.Asn658=
NM_172057.2:c.953A= , LRG_288t3:c.953A=	NP_742054.1:p.Asn318=
XM_011516185.1:c.1673A=	XP_011514487.1:p.Asn558=
XM_011516186.1:c.1973A=	XP_011514488.1:p.Asn658=
XM_011516185.2:c.1673A=	XP_011514487.1:p.Asn558=
XM_011516186.3:c.1973A=	XP_011514488.1:p.Asn658=
XM_017012195.1:c.1823A=	XP_016867684.1:p.Asn608=
XM_017012196.1:c.1796A=	XP_016867685.1:p.Asn599=
NM_000238.4:c.1973A= MANE Select	NP_000229.1:p.Asn658=
NM_001204798.2:c.953A=	NP_001191727.1:p.Asn318=
NM_172057.3:c.953A=	NP_742054.1:p.Asn318=