Canonical Allele Identifier: CA458871218

Gene: KCNH2

Linked Data

• gnomAD v4: 7-150950220-G-T
• MyVariant Identifiers: chr7:g.150647308G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950220G>T , CM000669.2:g.150950220G>T	GRCh38
NC_000007.13:g.150647308G>T , CM000669.1:g.150647308G>T	GRCh37
NC_000007.12:g.150278241G>T	NCBI36
NG_008916.1:g.32707C>A , LRG_288:g.32707C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.1644C>A
ENST00000684241.1:n.3179C>A
ENST00000262186.10:c.2346C>A MANE Select	ENSP00000262186.5:p.Ile782=
ENST00000330883.9:c.1326C>A	ENSP00000328531.4:p.Ile442=
ENST00000262186.9:c.2346C>A	ENSP00000262186.5:p.Ile782=
ENST00000330883.8:c.1326C>A	ENSP00000328531.4:p.Ile442=
ENST00000430723.4:c.1998C>A	ENSP00000387657.4:p.Ile666=
ENST00000461280.1:n.1633C>A
ENST00000473610.5:n.1978C>A
ENST00000532957.5:n.2569C>A
NM_000238.3:c.2346C>A , LRG_288t1:c.2346C>A	NP_000229.1:p.Ile782=
NM_001204798.1:c.1326C>A	NP_001191727.1:p.Ile442=
NM_172056.2:c.2346C>A , LRG_288t2:c.2346C>A	NP_742053.1:p.Ile782=
NM_172057.2:c.1326C>A , LRG_288t3:c.1326C>A	NP_742054.1:p.Ile442=
XM_011516185.1:c.2046C>A	XP_011514487.1:p.Ile682=
XM_011516186.1:c.2346C>A	XP_011514488.1:p.Ile782=
XM_011516185.2:c.2046C>A	XP_011514487.1:p.Ile682=
XM_011516186.3:c.2346C>A	XP_011514488.1:p.Ile782=
XM_017012195.1:c.2196C>A	XP_016867684.1:p.Ile732=
XM_017012196.1:c.2169C>A	XP_016867685.1:p.Ile723=
NM_000238.4:c.2346C>A MANE Select	NP_000229.1:p.Ile782=
NM_001204798.2:c.1326C>A	NP_001191727.1:p.Ile442=
NM_172057.3:c.1326C>A	NP_742054.1:p.Ile442=