Canonical Allele Identifier: CA1752409437

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951490T= , CM000669.2:g.150951490T=	GRCh38
NC_000007.13:g.150648578T= , CM000669.1:g.150648578T=	GRCh37
NC_000007.12:g.150279511T=	NCBI36
NG_008916.1:g.31437A= , LRG_288:g.31437A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1201A=
ENST00000683359.1:n.27A=
ENST00000684241.1:n.2736A=
ENST00000262186.10:c.1903A= MANE Select	ENSP00000262186.5:p.Asn635=
ENST00000330883.9:c.883A=	ENSP00000328531.4:p.Asn295=
ENST00000262186.9:c.1903A=	ENSP00000262186.5:p.Asn635=
ENST00000330883.8:c.883A=	ENSP00000328531.4:p.Asn295=
ENST00000430723.4:c.1555A=	ENSP00000387657.4:p.Asn519=
ENST00000461280.1:n.1190A=
ENST00000473610.5:n.1208A=
ENST00000532957.5:n.2126A=
NM_000238.3:c.1903A= , LRG_288t1:c.1903A=	NP_000229.1:p.Asn635=
NM_001204798.1:c.883A=	NP_001191727.1:p.Asn295=
NM_172056.2:c.1903A= , LRG_288t2:c.1903A=	NP_742053.1:p.Asn635=
NM_172057.2:c.883A= , LRG_288t3:c.883A=	NP_742054.1:p.Asn295=
XM_011516185.1:c.1603A=	XP_011514487.1:p.Asn535=
XM_011516186.1:c.1903A=	XP_011514488.1:p.Asn635=
XM_011516185.2:c.1603A=	XP_011514487.1:p.Asn535=
XM_011516186.3:c.1903A=	XP_011514488.1:p.Asn635=
XM_017012195.1:c.1753A=	XP_016867684.1:p.Asn585=
XM_017012196.1:c.1726A=	XP_016867685.1:p.Asn576=
NM_000238.4:c.1903A= MANE Select	NP_000229.1:p.Asn635=
NM_001204798.2:c.883A=	NP_001191727.1:p.Asn295=
NM_172057.3:c.883A=	NP_742054.1:p.Asn295=