Canonical Allele Identifier: CA369857530

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648085G>T (hg19) ; chr7:g.150950997G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150950997G>T , CM000669.2:g.150950997G>T	GRCh38
NC_000007.13:g.150648085G>T , CM000669.1:g.150648085G>T	GRCh37
NC_000007.12:g.150279018G>T	NCBI36
NG_008916.1:g.31930C>A , LRG_288:g.31930C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.1367C>A
ENST00000683359.1:n.193C>A
ENST00000684241.1:n.2902C>A
ENST00000262186.10:c.2069C>A MANE Select	ENSP00000262186.5:p.Pro690His
ENST00000330883.9:c.1049C>A	ENSP00000328531.4:p.Pro350His
ENST00000262186.9:c.2069C>A	ENSP00000262186.5:p.Pro690His
ENST00000330883.8:c.1049C>A	ENSP00000328531.4:p.Pro350His
ENST00000430723.4:c.1721C>A	ENSP00000387657.4:p.Pro574His
ENST00000461280.1:n.1356C>A
ENST00000473610.5:n.1701C>A
ENST00000532957.5:n.2292C>A
NM_000238.3:c.2069C>A , LRG_288t1:c.2069C>A	NP_000229.1:p.Pro690His
NM_001204798.1:c.1049C>A	NP_001191727.1:p.Pro350His
NM_172056.2:c.2069C>A , LRG_288t2:c.2069C>A	NP_742053.1:p.Pro690His
NM_172057.2:c.1049C>A , LRG_288t3:c.1049C>A	NP_742054.1:p.Pro350His
XM_011516185.1:c.1769C>A	XP_011514487.1:p.Pro590His
XM_011516186.1:c.2069C>A	XP_011514488.1:p.Pro690His
XM_011516185.2:c.1769C>A	XP_011514487.1:p.Pro590His
XM_011516186.3:c.2069C>A	XP_011514488.1:p.Pro690His
XM_017012195.1:c.1919C>A	XP_016867684.1:p.Pro640His
XM_017012196.1:c.1892C>A	XP_016867685.1:p.Pro631His
NM_000238.4:c.2069C>A MANE Select	NP_000229.1:p.Pro690His
NM_001204798.2:c.1049C>A	NP_001191727.1:p.Pro350His
NM_172057.3:c.1049C>A	NP_742054.1:p.Pro350His