Canonical Allele Identifier: CA369857725

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 3016546
• ClinVar RCV Id: RCV003878681
• MyVariant Identifiers: chr7:g.150648178A>C (hg19) ; chr7:g.150951090A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951090A>C , CM000669.2:g.150951090A>C	GRCh38
NC_000007.13:g.150648178A>C , CM000669.1:g.150648178A>C	GRCh37
NC_000007.12:g.150279111A>C	NCBI36
NG_008916.1:g.31837T>G , LRG_288:g.31837T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1274T>G
ENST00000683359.1:n.100T>G
ENST00000684241.1:n.2809T>G
ENST00000262186.10:c.1976T>G MANE Select	ENSP00000262186.5:p.Val659Gly
ENST00000330883.9:c.956T>G	ENSP00000328531.4:p.Val319Gly
ENST00000262186.9:c.1976T>G	ENSP00000262186.5:p.Val659Gly
ENST00000330883.8:c.956T>G	ENSP00000328531.4:p.Val319Gly
ENST00000430723.4:c.1628T>G	ENSP00000387657.4:p.Val543Gly
ENST00000461280.1:n.1263T>G
ENST00000473610.5:n.1608T>G
ENST00000532957.5:n.2199T>G
NM_000238.3:c.1976T>G , LRG_288t1:c.1976T>G	NP_000229.1:p.Val659Gly
NM_001204798.1:c.956T>G	NP_001191727.1:p.Val319Gly
NM_172056.2:c.1976T>G , LRG_288t2:c.1976T>G	NP_742053.1:p.Val659Gly
NM_172057.2:c.956T>G , LRG_288t3:c.956T>G	NP_742054.1:p.Val319Gly
XM_011516185.1:c.1676T>G	XP_011514487.1:p.Val559Gly
XM_011516186.1:c.1976T>G	XP_011514488.1:p.Val659Gly
XM_011516185.2:c.1676T>G	XP_011514487.1:p.Val559Gly
XM_011516186.3:c.1976T>G	XP_011514488.1:p.Val659Gly
XM_017012195.1:c.1826T>G	XP_016867684.1:p.Val609Gly
XM_017012196.1:c.1799T>G	XP_016867685.1:p.Val600Gly
NM_000238.4:c.1976T>G MANE Select	NP_000229.1:p.Val659Gly
NM_001204798.2:c.956T>G	NP_001191727.1:p.Val319Gly
NM_172057.3:c.956T>G	NP_742054.1:p.Val319Gly