Canonical Allele Identifier: CA005690

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 67297
• ClinVar RCV Id: RCV000058015 ; RCV001376739 ; RCV002408565
• dbSNP Id: rs199472947
• MyVariant Identifiers: chr7:g.150648628G>A (hg19) ; chr7:g.150951540G>A (hg38)
• PubMed: PMID:21130771 ; PMID:22581653

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951540G>A , CM000669.2:g.150951540G>A	GRCh38
NC_000007.13:g.150648628G>A , CM000669.1:g.150648628G>A	GRCh37
NC_000007.12:g.150279561G>A	NCBI36
NG_008916.1:g.31387C>T , LRG_288:g.31387C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1151C>T
ENST00000684241.1:n.2686C>T
ENST00000262186.10:c.1853C>T MANE Select	ENSP00000262186.5:p.Thr618Ile
ENST00000330883.9:c.833C>T	ENSP00000328531.4:p.Thr278Ile
ENST00000262186.9:c.1853C>T	ENSP00000262186.5:p.Thr618Ile
ENST00000330883.8:c.833C>T	ENSP00000328531.4:p.Thr278Ile
ENST00000430723.4:c.1505C>T	ENSP00000387657.4:p.Thr502Ile
ENST00000461280.1:n.1140C>T
ENST00000473610.5:n.1158C>T
ENST00000532957.5:n.2076C>T
NM_000238.3:c.1853C>T , LRG_288t1:c.1853C>T	NP_000229.1:p.Thr618Ile
NM_001204798.1:c.833C>T	NP_001191727.1:p.Thr278Ile
NM_172056.2:c.1853C>T , LRG_288t2:c.1853C>T	NP_742053.1:p.Thr618Ile
NM_172057.2:c.833C>T , LRG_288t3:c.833C>T	NP_742054.1:p.Thr278Ile
XM_011516185.1:c.1553C>T	XP_011514487.1:p.Thr518Ile
XM_011516186.1:c.1853C>T	XP_011514488.1:p.Thr618Ile
XM_011516185.2:c.1553C>T	XP_011514487.1:p.Thr518Ile
XM_011516186.3:c.1853C>T	XP_011514488.1:p.Thr618Ile
XM_017012195.1:c.1703C>T	XP_016867684.1:p.Thr568Ile
XM_017012196.1:c.1676C>T	XP_016867685.1:p.Thr559Ile
NM_000238.4:c.1853C>T MANE Select	NP_000229.1:p.Thr618Ile
NM_001204798.2:c.833C>T	NP_001191727.1:p.Thr278Ile
NM_172057.3:c.833C>T	NP_742054.1:p.Thr278Ile