Canonical Allele Identifier: CA458871363

Gene: KCNH2

Linked Data

• ClinVar Variation Id: 3071267
• ClinVar RCV Id: RCV004014769
• MyVariant Identifiers: chr7:g.150647416G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950328G>A , CM000669.2:g.150950328G>A	GRCh38
NC_000007.13:g.150647416G>A , CM000669.1:g.150647416G>A	GRCh37
NC_000007.12:g.150278349G>A	NCBI36
NG_008916.1:g.32599C>T , LRG_288:g.32599C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1536C>T
ENST00000684241.1:n.3071C>T
ENST00000262186.10:c.2238C>T MANE Select	ENSP00000262186.5:p.Ala746=
ENST00000330883.9:c.1218C>T	ENSP00000328531.4:p.Ala406=
ENST00000262186.9:c.2238C>T	ENSP00000262186.5:p.Ala746=
ENST00000330883.8:c.1218C>T	ENSP00000328531.4:p.Ala406=
ENST00000430723.4:c.1890C>T	ENSP00000387657.4:p.Ala630=
ENST00000461280.1:n.1525C>T
ENST00000473610.5:n.1870C>T
ENST00000532957.5:n.2461C>T
NM_000238.3:c.2238C>T , LRG_288t1:c.2238C>T	NP_000229.1:p.Ala746=
NM_001204798.1:c.1218C>T	NP_001191727.1:p.Ala406=
NM_172056.2:c.2238C>T , LRG_288t2:c.2238C>T	NP_742053.1:p.Ala746=
NM_172057.2:c.1218C>T , LRG_288t3:c.1218C>T	NP_742054.1:p.Ala406=
XM_011516185.1:c.1938C>T	XP_011514487.1:p.Ala646=
XM_011516186.1:c.2238C>T	XP_011514488.1:p.Ala746=
XM_011516185.2:c.1938C>T	XP_011514487.1:p.Ala646=
XM_011516186.3:c.2238C>T	XP_011514488.1:p.Ala746=
XM_017012195.1:c.2088C>T	XP_016867684.1:p.Ala696=
XM_017012196.1:c.2061C>T	XP_016867685.1:p.Ala687=
NM_000238.4:c.2238C>T MANE Select	NP_000229.1:p.Ala746=
NM_001204798.2:c.1218C>T	NP_001191727.1:p.Ala406=
NM_172057.3:c.1218C>T	NP_742054.1:p.Ala406=