Canonical Allele Identifier: CA006114

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 67348
• ClinVar RCV Id: RCV000058068 ; RCV000205745 ; RCV003162442
• dbSNP Id: rs199472978
• COSMIC: COSM5406963 ; COSM5406964 ; COSM5406965
• MyVariant Identifiers: chr7:g.150648185C>T (hg19) ; chr7:g.150951097C>T (hg38)
• PubMed: PMID:19716085 ; PMID:22581653

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951097C>T , CM000669.2:g.150951097C>T	GRCh38
NC_000007.13:g.150648185C>T , CM000669.1:g.150648185C>T	GRCh37
NC_000007.12:g.150279118C>T	NCBI36
NG_008916.1:g.31830G>A , LRG_288:g.31830G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.1267G>A
ENST00000683359.1:n.93G>A
ENST00000684241.1:n.2802G>A
ENST00000262186.10:c.1969G>A MANE Select	ENSP00000262186.5:p.Gly657Ser
ENST00000330883.9:c.949G>A	ENSP00000328531.4:p.Gly317Ser
ENST00000262186.9:c.1969G>A	ENSP00000262186.5:p.Gly657Ser
ENST00000330883.8:c.949G>A	ENSP00000328531.4:p.Gly317Ser
ENST00000430723.4:c.1621G>A	ENSP00000387657.4:p.Gly541Ser
ENST00000461280.1:n.1256G>A
ENST00000473610.5:n.1601G>A
ENST00000532957.5:n.2192G>A
NM_000238.3:c.1969G>A , LRG_288t1:c.1969G>A	NP_000229.1:p.Gly657Ser
NM_001204798.1:c.949G>A	NP_001191727.1:p.Gly317Ser
NM_172056.2:c.1969G>A , LRG_288t2:c.1969G>A	NP_742053.1:p.Gly657Ser
NM_172057.2:c.949G>A , LRG_288t3:c.949G>A	NP_742054.1:p.Gly317Ser
XM_011516185.1:c.1669G>A	XP_011514487.1:p.Gly557Ser
XM_011516186.1:c.1969G>A	XP_011514488.1:p.Gly657Ser
XM_011516185.2:c.1669G>A	XP_011514487.1:p.Gly557Ser
XM_011516186.3:c.1969G>A	XP_011514488.1:p.Gly657Ser
XM_017012195.1:c.1819G>A	XP_016867684.1:p.Gly607Ser
XM_017012196.1:c.1792G>A	XP_016867685.1:p.Gly598Ser
NM_000238.4:c.1969G>A MANE Select	NP_000229.1:p.Gly657Ser
NM_001204798.2:c.949G>A	NP_001191727.1:p.Gly317Ser
NM_172057.3:c.949G>A	NP_742054.1:p.Gly317Ser