Canonical Allele Identifier: CA458871607

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649582G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952494G>A , CM000669.2:g.150952494G>A	GRCh38
NC_000007.13:g.150649582G>A , CM000669.1:g.150649582G>A	GRCh37
NC_000007.12:g.150280515G>A	NCBI36
NG_008916.1:g.30433C>T , LRG_288:g.30433C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.786C>T
ENST00000684116.1:n.381C>T
ENST00000684241.1:n.2321C>T
ENST00000262186.10:c.1488C>T MANE Select	ENSP00000262186.5:p.Gly496=
ENST00000330883.9:c.468C>T	ENSP00000328531.4:p.Gly156=
ENST00000262186.9:c.1488C>T	ENSP00000262186.5:p.Gly496=
ENST00000330883.8:c.468C>T	ENSP00000328531.4:p.Gly156=
ENST00000430723.4:c.1140C>T	ENSP00000387657.4:p.Gly380=
ENST00000461280.1:n.775C>T
ENST00000473610.5:n.793C>T
ENST00000532957.5:n.1711C>T
NM_000238.3:c.1488C>T , LRG_288t1:c.1488C>T	NP_000229.1:p.Gly496=
NM_001204798.1:c.468C>T	NP_001191727.1:p.Gly156=
NM_172056.2:c.1488C>T , LRG_288t2:c.1488C>T	NP_742053.1:p.Gly496=
NM_172057.2:c.468C>T , LRG_288t3:c.468C>T	NP_742054.1:p.Gly156=
XM_011516185.1:c.1188C>T	XP_011514487.1:p.Gly396=
XM_011516186.1:c.1488C>T	XP_011514488.1:p.Gly496=
XM_011516185.2:c.1188C>T	XP_011514487.1:p.Gly396=
XM_011516186.3:c.1488C>T	XP_011514488.1:p.Gly496=
XM_017012195.1:c.1338C>T	XP_016867684.1:p.Gly446=
XM_017012196.1:c.1311C>T	XP_016867685.1:p.Gly437=
NM_000238.4:c.1488C>T MANE Select	NP_000229.1:p.Gly496=
NM_001204798.2:c.468C>T	NP_001191727.1:p.Gly156=
NM_172057.3:c.468C>T	NP_742054.1:p.Gly156=