Canonical Allele Identifier: CA369859630

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649572T>A (hg19) ; chr7:g.150952484T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952484T>A , CM000669.2:g.150952484T>A	GRCh38
NC_000007.13:g.150649572T>A , CM000669.1:g.150649572T>A	GRCh37
NC_000007.12:g.150280505T>A	NCBI36
NG_008916.1:g.30443A>T , LRG_288:g.30443A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.796A>T
ENST00000684116.1:n.391A>T
ENST00000684241.1:n.2331A>T
ENST00000262186.10:c.1498A>T MANE Select	ENSP00000262186.5:p.Ile500Phe
ENST00000330883.9:c.478A>T	ENSP00000328531.4:p.Ile160Phe
ENST00000262186.9:c.1498A>T	ENSP00000262186.5:p.Ile500Phe
ENST00000330883.8:c.478A>T	ENSP00000328531.4:p.Ile160Phe
ENST00000430723.4:c.1150A>T	ENSP00000387657.4:p.Ile384Phe
ENST00000461280.1:n.785A>T
ENST00000473610.5:n.803A>T
ENST00000532957.5:n.1721A>T
NM_000238.3:c.1498A>T , LRG_288t1:c.1498A>T	NP_000229.1:p.Ile500Phe
NM_001204798.1:c.478A>T	NP_001191727.1:p.Ile160Phe
NM_172056.2:c.1498A>T , LRG_288t2:c.1498A>T	NP_742053.1:p.Ile500Phe
NM_172057.2:c.478A>T , LRG_288t3:c.478A>T	NP_742054.1:p.Ile160Phe
XM_011516185.1:c.1198A>T	XP_011514487.1:p.Ile400Phe
XM_011516186.1:c.1498A>T	XP_011514488.1:p.Ile500Phe
XM_011516185.2:c.1198A>T	XP_011514487.1:p.Ile400Phe
XM_011516186.3:c.1498A>T	XP_011514488.1:p.Ile500Phe
XM_017012195.1:c.1348A>T	XP_016867684.1:p.Ile450Phe
XM_017012196.1:c.1321A>T	XP_016867685.1:p.Ile441Phe
NM_000238.4:c.1498A>T MANE Select	NP_000229.1:p.Ile500Phe
NM_001204798.2:c.478A>T	NP_001191727.1:p.Ile160Phe
NM_172057.3:c.478A>T	NP_742054.1:p.Ile160Phe