Canonical Allele Identifier: CA005087

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 67234
• ClinVar RCV Id: RCV000057945
• dbSNP Id: rs199473517
• MyVariant Identifiers: chr7:g.150648792C>A (hg19) ; chr7:g.150951704C>A (hg38)
• PubMed: PMID:19926013 ; PMID:22581653

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951704C>A , CM000669.2:g.150951704C>A	GRCh38
NC_000007.13:g.150648792C>A , CM000669.1:g.150648792C>A	GRCh37
NC_000007.12:g.150279725C>A	NCBI36
NG_008916.1:g.31223G>T , LRG_288:g.31223G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.987G>T
ENST00000684241.1:n.2522G>T
ENST00000262186.10:c.1689G>T MANE Select	ENSP00000262186.5:p.Trp563Cys
ENST00000330883.9:c.669G>T	ENSP00000328531.4:p.Trp223Cys
ENST00000262186.9:c.1689G>T	ENSP00000262186.5:p.Trp563Cys
ENST00000330883.8:c.669G>T	ENSP00000328531.4:p.Trp223Cys
ENST00000430723.4:c.1341G>T	ENSP00000387657.4:p.Trp447Cys
ENST00000461280.1:n.976G>T
ENST00000473610.5:n.994G>T
ENST00000532957.5:n.1912G>T
NM_000238.3:c.1689G>T , LRG_288t1:c.1689G>T	NP_000229.1:p.Trp563Cys
NM_001204798.1:c.669G>T	NP_001191727.1:p.Trp223Cys
NM_172056.2:c.1689G>T , LRG_288t2:c.1689G>T	NP_742053.1:p.Trp563Cys
NM_172057.2:c.669G>T , LRG_288t3:c.669G>T	NP_742054.1:p.Trp223Cys
XM_011516185.1:c.1389G>T	XP_011514487.1:p.Trp463Cys
XM_011516186.1:c.1689G>T	XP_011514488.1:p.Trp563Cys
XM_011516185.2:c.1389G>T	XP_011514487.1:p.Trp463Cys
XM_011516186.3:c.1689G>T	XP_011514488.1:p.Trp563Cys
XM_017012195.1:c.1539G>T	XP_016867684.1:p.Trp513Cys
XM_017012196.1:c.1512G>T	XP_016867685.1:p.Trp504Cys
NM_000238.4:c.1689G>T MANE Select	NP_000229.1:p.Trp563Cys
NM_001204798.2:c.669G>T	NP_001191727.1:p.Trp223Cys
NM_172057.3:c.669G>T	NP_742054.1:p.Trp223Cys