Canonical Allele Identifier: CA458871695

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649744A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952656A>T , CM000669.2:g.150952656A>T	GRCh38
NC_000007.13:g.150649744A>T , CM000669.1:g.150649744A>T	GRCh37
NC_000007.12:g.150280677A>T	NCBI36
NG_008916.1:g.30271T>A , LRG_288:g.30271T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.624T>A
ENST00000684116.1:n.219T>A
ENST00000684241.1:n.2159T>A
ENST00000262186.10:c.1326T>A MANE Select	ENSP00000262186.5:p.Ala442=
ENST00000330883.9:c.306T>A	ENSP00000328531.4:p.Ala102=
ENST00000262186.9:c.1326T>A	ENSP00000262186.5:p.Ala442=
ENST00000330883.8:c.306T>A	ENSP00000328531.4:p.Ala102=
ENST00000430723.4:c.978T>A	ENSP00000387657.4:p.Ala326=
ENST00000461280.1:n.613T>A
ENST00000473610.5:n.631T>A
ENST00000532957.5:n.1549T>A
NM_000238.3:c.1326T>A , LRG_288t1:c.1326T>A	NP_000229.1:p.Ala442=
NM_001204798.1:c.306T>A	NP_001191727.1:p.Ala102=
NM_172056.2:c.1326T>A , LRG_288t2:c.1326T>A	NP_742053.1:p.Ala442=
NM_172057.2:c.306T>A , LRG_288t3:c.306T>A	NP_742054.1:p.Ala102=
XM_011516185.1:c.1026T>A	XP_011514487.1:p.Ala342=
XM_011516186.1:c.1326T>A	XP_011514488.1:p.Ala442=
XM_011516185.2:c.1026T>A	XP_011514487.1:p.Ala342=
XM_011516186.3:c.1326T>A	XP_011514488.1:p.Ala442=
XM_017012195.1:c.1176T>A	XP_016867684.1:p.Ala392=
XM_017012196.1:c.1149T>A	XP_016867685.1:p.Ala383=
NM_000238.4:c.1326T>A MANE Select	NP_000229.1:p.Ala442=
NM_001204798.2:c.306T>A	NP_001191727.1:p.Ala102=
NM_172057.3:c.306T>A	NP_742054.1:p.Ala102=