Canonical Allele Identifier: CA369859663

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649586T>A (hg19) ; chr7:g.150952498T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952498T>A , CM000669.2:g.150952498T>A	GRCh38
NC_000007.13:g.150649586T>A , CM000669.1:g.150649586T>A	GRCh37
NC_000007.12:g.150280519T>A	NCBI36
NG_008916.1:g.30429A>T , LRG_288:g.30429A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.782A>T
ENST00000684116.1:n.377A>T
ENST00000684241.1:n.2317A>T
ENST00000262186.10:c.1484A>T MANE Select	ENSP00000262186.5:p.Lys495Met
ENST00000330883.9:c.464A>T	ENSP00000328531.4:p.Lys155Met
ENST00000262186.9:c.1484A>T	ENSP00000262186.5:p.Lys495Met
ENST00000330883.8:c.464A>T	ENSP00000328531.4:p.Lys155Met
ENST00000430723.4:c.1136A>T	ENSP00000387657.4:p.Lys379Met
ENST00000461280.1:n.771A>T
ENST00000473610.5:n.789A>T
ENST00000532957.5:n.1707A>T
NM_000238.3:c.1484A>T , LRG_288t1:c.1484A>T	NP_000229.1:p.Lys495Met
NM_001204798.1:c.464A>T	NP_001191727.1:p.Lys155Met
NM_172056.2:c.1484A>T , LRG_288t2:c.1484A>T	NP_742053.1:p.Lys495Met
NM_172057.2:c.464A>T , LRG_288t3:c.464A>T	NP_742054.1:p.Lys155Met
XM_011516185.1:c.1184A>T	XP_011514487.1:p.Lys395Met
XM_011516186.1:c.1484A>T	XP_011514488.1:p.Lys495Met
XM_011516185.2:c.1184A>T	XP_011514487.1:p.Lys395Met
XM_011516186.3:c.1484A>T	XP_011514488.1:p.Lys495Met
XM_017012195.1:c.1334A>T	XP_016867684.1:p.Lys445Met
XM_017012196.1:c.1307A>T	XP_016867685.1:p.Lys436Met
NM_000238.4:c.1484A>T MANE Select	NP_000229.1:p.Lys495Met
NM_001204798.2:c.464A>T	NP_001191727.1:p.Lys155Met
NM_172057.3:c.464A>T	NP_742054.1:p.Lys155Met