Canonical Allele Identifier: CA005780

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 67309
• ClinVar RCV Id: RCV000058027 ; RCV002513755
• dbSNP Id: rs199472954
• MyVariant Identifiers: chr7:g.150648602A>G (hg19) ; chr7:g.150951514A>G (hg38)
• PubMed: PMID:18848812 ; PMID:22581653

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951514A>G , CM000669.2:g.150951514A>G	GRCh38
NC_000007.13:g.150648602A>G , CM000669.1:g.150648602A>G	GRCh37
NC_000007.12:g.150279535A>G	NCBI36
NG_008916.1:g.31413T>C , LRG_288:g.31413T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1177T>C
ENST00000683359.1:n.3T>C
ENST00000684241.1:n.2712T>C
ENST00000262186.10:c.1879T>C MANE Select	ENSP00000262186.5:p.Phe627Leu
ENST00000330883.9:c.859T>C	ENSP00000328531.4:p.Phe287Leu
ENST00000262186.9:c.1879T>C	ENSP00000262186.5:p.Phe627Leu
ENST00000330883.8:c.859T>C	ENSP00000328531.4:p.Phe287Leu
ENST00000430723.4:c.1531T>C	ENSP00000387657.4:p.Phe511Leu
ENST00000461280.1:n.1166T>C
ENST00000473610.5:n.1184T>C
ENST00000532957.5:n.2102T>C
NM_000238.3:c.1879T>C , LRG_288t1:c.1879T>C	NP_000229.1:p.Phe627Leu
NM_001204798.1:c.859T>C	NP_001191727.1:p.Phe287Leu
NM_172056.2:c.1879T>C , LRG_288t2:c.1879T>C	NP_742053.1:p.Phe627Leu
NM_172057.2:c.859T>C , LRG_288t3:c.859T>C	NP_742054.1:p.Phe287Leu
XM_011516185.1:c.1579T>C	XP_011514487.1:p.Phe527Leu
XM_011516186.1:c.1879T>C	XP_011514488.1:p.Phe627Leu
XM_011516185.2:c.1579T>C	XP_011514487.1:p.Phe527Leu
XM_011516186.3:c.1879T>C	XP_011514488.1:p.Phe627Leu
XM_017012195.1:c.1729T>C	XP_016867684.1:p.Phe577Leu
XM_017012196.1:c.1702T>C	XP_016867685.1:p.Phe568Leu
NM_000238.4:c.1879T>C MANE Select	NP_000229.1:p.Phe627Leu
NM_001204798.2:c.859T>C	NP_001191727.1:p.Phe287Leu
NM_172057.3:c.859T>C	NP_742054.1:p.Phe287Leu