Canonical Allele Identifier: CA005051

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 200733
• ClinVar RCV Id: RCV000182026 ; RCV000531749
• dbSNP Id: rs794728481
• MyVariant Identifiers: chr7:g.150648797G>A (hg19) ; chr7:g.150951709G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951709G>A , CM000669.2:g.150951709G>A	GRCh38
NC_000007.13:g.150648797G>A , CM000669.1:g.150648797G>A	GRCh37
NC_000007.12:g.150279730G>A	NCBI36
NG_008916.1:g.31218C>T , LRG_288:g.31218C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.982C>T
ENST00000684241.1:n.2517C>T
ENST00000262186.10:c.1684C>T MANE Select	ENSP00000262186.5:p.His562Tyr
ENST00000330883.9:c.664C>T	ENSP00000328531.4:p.His222Tyr
ENST00000262186.9:c.1684C>T	ENSP00000262186.5:p.His562Tyr
ENST00000330883.8:c.664C>T	ENSP00000328531.4:p.His222Tyr
ENST00000430723.4:c.1336C>T	ENSP00000387657.4:p.His446Tyr
ENST00000461280.1:n.971C>T
ENST00000473610.5:n.989C>T
ENST00000532957.5:n.1907C>T
NM_000238.3:c.1684C>T , LRG_288t1:c.1684C>T	NP_000229.1:p.His562Tyr
NM_001204798.1:c.664C>T	NP_001191727.1:p.His222Tyr
NM_172056.2:c.1684C>T , LRG_288t2:c.1684C>T	NP_742053.1:p.His562Tyr
NM_172057.2:c.664C>T , LRG_288t3:c.664C>T	NP_742054.1:p.His222Tyr
XM_011516185.1:c.1384C>T	XP_011514487.1:p.His462Tyr
XM_011516186.1:c.1684C>T	XP_011514488.1:p.His562Tyr
XM_011516185.2:c.1384C>T	XP_011514487.1:p.His462Tyr
XM_011516186.3:c.1684C>T	XP_011514488.1:p.His562Tyr
XM_017012195.1:c.1534C>T	XP_016867684.1:p.His512Tyr
XM_017012196.1:c.1507C>T	XP_016867685.1:p.His503Tyr
NM_000238.4:c.1684C>T MANE Select	NP_000229.1:p.His562Tyr
NM_001204798.2:c.664C>T	NP_001191727.1:p.His222Tyr
NM_172057.3:c.664C>T	NP_742054.1:p.His222Tyr