Canonical Allele Identifier: CA369859794

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 811073
• ClinVar RCV Id: RCV001000688
• dbSNP Id: rs199472905
• MyVariant Identifiers: chr7:g.150649652G>A (hg19) ; chr7:g.150952564G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952564G>A , CM000669.2:g.150952564G>A	GRCh38
NC_000007.13:g.150649652G>A , CM000669.1:g.150649652G>A	GRCh37
NC_000007.12:g.150280585G>A	NCBI36
NG_008916.1:g.30363C>T , LRG_288:g.30363C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.716C>T
ENST00000684116.1:n.311C>T
ENST00000684241.1:n.2251C>T
ENST00000262186.10:c.1418C>T MANE Select	ENSP00000262186.5:p.Thr473Ile
ENST00000330883.9:c.398C>T	ENSP00000328531.4:p.Thr133Ile
ENST00000262186.9:c.1418C>T	ENSP00000262186.5:p.Thr473Ile
ENST00000330883.8:c.398C>T	ENSP00000328531.4:p.Thr133Ile
ENST00000430723.4:c.1070C>T	ENSP00000387657.4:p.Thr357Ile
ENST00000461280.1:n.705C>T
ENST00000473610.5:n.723C>T
ENST00000532957.5:n.1641C>T
NM_000238.3:c.1418C>T , LRG_288t1:c.1418C>T	NP_000229.1:p.Thr473Ile
NM_001204798.1:c.398C>T	NP_001191727.1:p.Thr133Ile
NM_172056.2:c.1418C>T , LRG_288t2:c.1418C>T	NP_742053.1:p.Thr473Ile
NM_172057.2:c.398C>T , LRG_288t3:c.398C>T	NP_742054.1:p.Thr133Ile
XM_011516185.1:c.1118C>T	XP_011514487.1:p.Thr373Ile
XM_011516186.1:c.1418C>T	XP_011514488.1:p.Thr473Ile
XM_011516185.2:c.1118C>T	XP_011514487.1:p.Thr373Ile
XM_011516186.3:c.1418C>T	XP_011514488.1:p.Thr473Ile
XM_017012195.1:c.1268C>T	XP_016867684.1:p.Thr423Ile
XM_017012196.1:c.1241C>T	XP_016867685.1:p.Thr414Ile
NM_000238.4:c.1418C>T MANE Select	NP_000229.1:p.Thr473Ile
NM_001204798.2:c.398C>T	NP_001191727.1:p.Thr133Ile
NM_172057.3:c.398C>T	NP_742054.1:p.Thr133Ile