Canonical Allele Identifier: CA1752414895

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150955552G= , CM000669.2:g.150955552G=	GRCh38
NC_000007.13:g.150652640G= , CM000669.1:g.150652640G=	GRCh37
NC_000007.12:g.150283573G=	NCBI36
NG_008916.1:g.27375C= , LRG_288:g.27375C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.270C=
ENST00000684241.1:n.1961+1739C=
ENST00000262186.10:c.1128+1739C= MANE Select	ENSP00000262186.5:n.1128+1739C=
ENST00000330883.9:c.-49C=	ENSP00000328531.4:n.-49C=
ENST00000262186.9:c.1128+1739C=	ENSP00000262186.5:n.1128+1739C=
ENST00000330883.8:c.-49C=	ENSP00000328531.4:n.-49C=
ENST00000430723.4:c.780+1739C=	ENSP00000387657.4:n.780+1739C=
ENST00000461280.1:n.259C=
ENST00000473610.5:n.277C=
ENST00000532957.5:n.1351+1739C=
NM_000238.3:c.1128+1739C= , LRG_288t1:c.1128+1739C=	NP_000229.1:n.1128+1739C=
NM_001204798.1:c.-49C=	NP_001191727.1:n.-49C=
NM_172056.2:c.1128+1739C= , LRG_288t2:c.1128+1739C=	NP_742053.1:n.1128+1739C=
NM_172057.2:c.-49C= , LRG_288t3:c.-49C=	NP_742054.1:n.-49C=
XM_011516185.1:c.828+1739C=	XP_011514487.1:n.828+1739C=
XM_011516186.1:c.1128+1739C=	XP_011514488.1:n.1128+1739C=
XM_011516185.2:c.828+1739C=	XP_011514487.1:n.828+1739C=
XM_011516186.3:c.1128+1739C=	XP_011514488.1:n.1128+1739C=
XM_017012195.1:c.978+1739C=	XP_016867684.1:n.978+1739C=
XM_017012196.1:c.951+1739C=	XP_016867685.1:n.951+1739C=
NM_000238.4:c.1128+1739C= MANE Select	NP_000229.1:n.1128+1739C=
NM_001204798.2:c.-49C=	NP_001191727.1:n.-49C=
NM_172057.3:c.-49C=	NP_742054.1:n.-49C=