Canonical Allele Identifier: CA369856698

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150647489T>A (hg19) ; chr7:g.150950401T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950401T>A , CM000669.2:g.150950401T>A	GRCh38
NC_000007.13:g.150647489T>A , CM000669.1:g.150647489T>A	GRCh37
NC_000007.12:g.150278422T>A	NCBI36
NG_008916.1:g.32526A>T , LRG_288:g.32526A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1463A>T
ENST00000684241.1:n.2998A>T
ENST00000262186.10:c.2165A>T MANE Select	ENSP00000262186.5:p.Glu722Val
ENST00000330883.9:c.1145A>T	ENSP00000328531.4:p.Glu382Val
ENST00000262186.9:c.2165A>T	ENSP00000262186.5:p.Glu722Val
ENST00000330883.8:c.1145A>T	ENSP00000328531.4:p.Glu382Val
ENST00000430723.4:c.1817A>T	ENSP00000387657.4:p.Glu606Val
ENST00000461280.1:n.1452A>T
ENST00000473610.5:n.1797A>T
ENST00000532957.5:n.2388A>T
NM_000238.3:c.2165A>T , LRG_288t1:c.2165A>T	NP_000229.1:p.Glu722Val
NM_001204798.1:c.1145A>T	NP_001191727.1:p.Glu382Val
NM_172056.2:c.2165A>T , LRG_288t2:c.2165A>T	NP_742053.1:p.Glu722Val
NM_172057.2:c.1145A>T , LRG_288t3:c.1145A>T	NP_742054.1:p.Glu382Val
XM_011516185.1:c.1865A>T	XP_011514487.1:p.Glu622Val
XM_011516186.1:c.2165A>T	XP_011514488.1:p.Glu722Val
XM_011516185.2:c.1865A>T	XP_011514487.1:p.Glu622Val
XM_011516186.3:c.2165A>T	XP_011514488.1:p.Glu722Val
XM_017012195.1:c.2015A>T	XP_016867684.1:p.Glu672Val
XM_017012196.1:c.1988A>T	XP_016867685.1:p.Glu663Val
NM_000238.4:c.2165A>T MANE Select	NP_000229.1:p.Glu722Val
NM_001204798.2:c.1145A>T	NP_001191727.1:p.Glu382Val
NM_172057.3:c.1145A>T	NP_742054.1:p.Glu382Val