Canonical Allele Identifier: CA1752410003

Gene: KCNH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951583C= , CM000669.2:g.150951583C=	GRCh38
NC_000007.13:g.150648671C= , CM000669.1:g.150648671C=	GRCh37
NC_000007.12:g.150279604C=	NCBI36
NG_008916.1:g.31344G= , LRG_288:g.31344G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1108G=
ENST00000684241.1:n.2643G=
ENST00000262186.10:c.1810G= MANE Select	ENSP00000262186.5:p.Gly604=
ENST00000330883.9:c.790G=	ENSP00000328531.4:p.Gly264=
ENST00000262186.9:c.1810G=	ENSP00000262186.5:p.Gly604=
ENST00000330883.8:c.790G=	ENSP00000328531.4:p.Gly264=
ENST00000430723.4:c.1462G=	ENSP00000387657.4:p.Gly488=
ENST00000461280.1:n.1097G=
ENST00000473610.5:n.1115G=
ENST00000532957.5:n.2033G=
NM_000238.3:c.1810G= , LRG_288t1:c.1810G=	NP_000229.1:p.Gly604=
NM_001204798.1:c.790G=	NP_001191727.1:p.Gly264=
NM_172056.2:c.1810G= , LRG_288t2:c.1810G=	NP_742053.1:p.Gly604=
NM_172057.2:c.790G= , LRG_288t3:c.790G=	NP_742054.1:p.Gly264=
XM_011516185.1:c.1510G=	XP_011514487.1:p.Gly504=
XM_011516186.1:c.1810G=	XP_011514488.1:p.Gly604=
XM_011516185.2:c.1510G=	XP_011514487.1:p.Gly504=
XM_011516186.3:c.1810G=	XP_011514488.1:p.Gly604=
XM_017012195.1:c.1660G=	XP_016867684.1:p.Gly554=
XM_017012196.1:c.1633G=	XP_016867685.1:p.Gly545=
NM_000238.4:c.1810G= MANE Select	NP_000229.1:p.Gly604=
NM_001204798.2:c.790G=	NP_001191727.1:p.Gly264=
NM_172057.3:c.790G=	NP_742054.1:p.Gly264=