Canonical Allele Identifier: CA458871609

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649585C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952497C>T , CM000669.2:g.150952497C>T	GRCh38
NC_000007.13:g.150649585C>T , CM000669.1:g.150649585C>T	GRCh37
NC_000007.12:g.150280518C>T	NCBI36
NG_008916.1:g.30430G>A , LRG_288:g.30430G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.783G>A
ENST00000684116.1:n.378G>A
ENST00000684241.1:n.2318G>A
ENST00000262186.10:c.1485G>A MANE Select	ENSP00000262186.5:p.Lys495=
ENST00000330883.9:c.465G>A	ENSP00000328531.4:p.Lys155=
ENST00000262186.9:c.1485G>A	ENSP00000262186.5:p.Lys495=
ENST00000330883.8:c.465G>A	ENSP00000328531.4:p.Lys155=
ENST00000430723.4:c.1137G>A	ENSP00000387657.4:p.Lys379=
ENST00000461280.1:n.772G>A
ENST00000473610.5:n.790G>A
ENST00000532957.5:n.1708G>A
NM_000238.3:c.1485G>A , LRG_288t1:c.1485G>A	NP_000229.1:p.Lys495=
NM_001204798.1:c.465G>A	NP_001191727.1:p.Lys155=
NM_172056.2:c.1485G>A , LRG_288t2:c.1485G>A	NP_742053.1:p.Lys495=
NM_172057.2:c.465G>A , LRG_288t3:c.465G>A	NP_742054.1:p.Lys155=
XM_011516185.1:c.1185G>A	XP_011514487.1:p.Lys395=
XM_011516186.1:c.1485G>A	XP_011514488.1:p.Lys495=
XM_011516185.2:c.1185G>A	XP_011514487.1:p.Lys395=
XM_011516186.3:c.1485G>A	XP_011514488.1:p.Lys495=
XM_017012195.1:c.1335G>A	XP_016867684.1:p.Lys445=
XM_017012196.1:c.1308G>A	XP_016867685.1:p.Lys436=
NM_000238.4:c.1485G>A MANE Select	NP_000229.1:p.Lys495=
NM_001204798.2:c.465G>A	NP_001191727.1:p.Lys155=
NM_172057.3:c.465G>A	NP_742054.1:p.Lys155=