Canonical Allele Identifier: CA005914

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 200391
• ClinVar RCV Id: RCV000181826 ; RCV003314572
• dbSNP Id: rs794728377
• MyVariant Identifiers: chr7:g.150648581T>C (hg19) ; chr7:g.150951493T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951493T>C , CM000669.2:g.150951493T>C	GRCh38
NC_000007.13:g.150648581T>C , CM000669.1:g.150648581T>C	GRCh37
NC_000007.12:g.150279514T>C	NCBI36
NG_008916.1:g.31434A>G , LRG_288:g.31434A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1198A>G
ENST00000683359.1:n.24A>G
ENST00000684241.1:n.2733A>G
ENST00000262186.10:c.1900A>G MANE Select	ENSP00000262186.5:p.Thr634Ala
ENST00000330883.9:c.880A>G	ENSP00000328531.4:p.Thr294Ala
ENST00000262186.9:c.1900A>G	ENSP00000262186.5:p.Thr634Ala
ENST00000330883.8:c.880A>G	ENSP00000328531.4:p.Thr294Ala
ENST00000430723.4:c.1552A>G	ENSP00000387657.4:p.Thr518Ala
ENST00000461280.1:n.1187A>G
ENST00000473610.5:n.1205A>G
ENST00000532957.5:n.2123A>G
NM_000238.3:c.1900A>G , LRG_288t1:c.1900A>G	NP_000229.1:p.Thr634Ala
NM_001204798.1:c.880A>G	NP_001191727.1:p.Thr294Ala
NM_172056.2:c.1900A>G , LRG_288t2:c.1900A>G	NP_742053.1:p.Thr634Ala
NM_172057.2:c.880A>G , LRG_288t3:c.880A>G	NP_742054.1:p.Thr294Ala
XM_011516185.1:c.1600A>G	XP_011514487.1:p.Thr534Ala
XM_011516186.1:c.1900A>G	XP_011514488.1:p.Thr634Ala
XM_011516185.2:c.1600A>G	XP_011514487.1:p.Thr534Ala
XM_011516186.3:c.1900A>G	XP_011514488.1:p.Thr634Ala
XM_017012195.1:c.1750A>G	XP_016867684.1:p.Thr584Ala
XM_017012196.1:c.1723A>G	XP_016867685.1:p.Thr575Ala
NM_000238.4:c.1900A>G MANE Select	NP_000229.1:p.Thr634Ala
NM_001204798.2:c.880A>G	NP_001191727.1:p.Thr294Ala
NM_172057.3:c.880A>G	NP_742054.1:p.Thr294Ala