Canonical Allele Identifier: CA005660

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 67293
• ClinVar RCV Id: RCV000058011 ; RCV002470744
• dbSNP Id: rs199472945
• MyVariant Identifiers: chr7:g.150648638G>C (hg19) ; chr7:g.150951550G>C (hg38)
• PubMed: PMID:10973849 ; PMID:22581653

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951550G>C , CM000669.2:g.150951550G>C	GRCh38
NC_000007.13:g.150648638G>C , CM000669.1:g.150648638G>C	GRCh37
NC_000007.12:g.150279571G>C	NCBI36
NG_008916.1:g.31377C>G , LRG_288:g.31377C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1141C>G
ENST00000684241.1:n.2676C>G
ENST00000262186.10:c.1843C>G MANE Select	ENSP00000262186.5:p.Leu615Val
ENST00000330883.9:c.823C>G	ENSP00000328531.4:p.Leu275Val
ENST00000262186.9:c.1843C>G	ENSP00000262186.5:p.Leu615Val
ENST00000330883.8:c.823C>G	ENSP00000328531.4:p.Leu275Val
ENST00000430723.4:c.1495C>G	ENSP00000387657.4:p.Leu499Val
ENST00000461280.1:n.1130C>G
ENST00000473610.5:n.1148C>G
ENST00000532957.5:n.2066C>G
NM_000238.3:c.1843C>G , LRG_288t1:c.1843C>G	NP_000229.1:p.Leu615Val
NM_001204798.1:c.823C>G	NP_001191727.1:p.Leu275Val
NM_172056.2:c.1843C>G , LRG_288t2:c.1843C>G	NP_742053.1:p.Leu615Val
NM_172057.2:c.823C>G , LRG_288t3:c.823C>G	NP_742054.1:p.Leu275Val
XM_011516185.1:c.1543C>G	XP_011514487.1:p.Leu515Val
XM_011516186.1:c.1843C>G	XP_011514488.1:p.Leu615Val
XM_011516185.2:c.1543C>G	XP_011514487.1:p.Leu515Val
XM_011516186.3:c.1843C>G	XP_011514488.1:p.Leu615Val
XM_017012195.1:c.1693C>G	XP_016867684.1:p.Leu565Val
XM_017012196.1:c.1666C>G	XP_016867685.1:p.Leu556Val
NM_000238.4:c.1843C>G MANE Select	NP_000229.1:p.Leu615Val
NM_001204798.2:c.823C>G	NP_001191727.1:p.Leu275Val
NM_172057.3:c.823C>G	NP_742054.1:p.Leu275Val