Canonical Allele Identifier: CA005864

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 67317
• ClinVar RCV Id: RCV000058036 ; RCV001854201
• dbSNP Id: rs41307295
• MyVariant Identifiers: chr7:g.150648594G>T (hg19) ; chr7:g.150951506G>T (hg38)
• PubMed: PMID:10517660 ; PMID:22581653

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951506G>T , CM000669.2:g.150951506G>T	GRCh38
NC_000007.13:g.150648594G>T , CM000669.1:g.150648594G>T	GRCh37
NC_000007.12:g.150279527G>T	NCBI36
NG_008916.1:g.31421C>A , LRG_288:g.31421C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1185C>A
ENST00000683359.1:n.11C>A
ENST00000684241.1:n.2720C>A
ENST00000262186.10:c.1887C>A MANE Select	ENSP00000262186.5:p.Asn629Lys
ENST00000330883.9:c.867C>A	ENSP00000328531.4:p.Asn289Lys
ENST00000262186.9:c.1887C>A	ENSP00000262186.5:p.Asn629Lys
ENST00000330883.8:c.867C>A	ENSP00000328531.4:p.Asn289Lys
ENST00000430723.4:c.1539C>A	ENSP00000387657.4:p.Asn513Lys
ENST00000461280.1:n.1174C>A
ENST00000473610.5:n.1192C>A
ENST00000532957.5:n.2110C>A
NM_000238.3:c.1887C>A , LRG_288t1:c.1887C>A	NP_000229.1:p.Asn629Lys
NM_001204798.1:c.867C>A	NP_001191727.1:p.Asn289Lys
NM_172056.2:c.1887C>A , LRG_288t2:c.1887C>A	NP_742053.1:p.Asn629Lys
NM_172057.2:c.867C>A , LRG_288t3:c.867C>A	NP_742054.1:p.Asn289Lys
XM_011516185.1:c.1587C>A	XP_011514487.1:p.Asn529Lys
XM_011516186.1:c.1887C>A	XP_011514488.1:p.Asn629Lys
XM_011516185.2:c.1587C>A	XP_011514487.1:p.Asn529Lys
XM_011516186.3:c.1887C>A	XP_011514488.1:p.Asn629Lys
XM_017012195.1:c.1737C>A	XP_016867684.1:p.Asn579Lys
XM_017012196.1:c.1710C>A	XP_016867685.1:p.Asn570Lys
NM_000238.4:c.1887C>A MANE Select	NP_000229.1:p.Asn629Lys
NM_001204798.2:c.867C>A	NP_001191727.1:p.Asn289Lys
NM_172057.3:c.867C>A	NP_742054.1:p.Asn289Lys