Canonical Allele Identifier: CA369860184

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649850T>A (hg19) ; chr7:g.150952762T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952762T>A , CM000669.2:g.150952762T>A	GRCh38
NC_000007.13:g.150649850T>A , CM000669.1:g.150649850T>A	GRCh37
NC_000007.12:g.150280783T>A	NCBI36
NG_008916.1:g.30165A>T , LRG_288:g.30165A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.518A>T
ENST00000684116.1:n.113A>T
ENST00000684241.1:n.2053A>T
ENST00000262186.10:c.1220A>T MANE Select	ENSP00000262186.5:p.Lys407Met
ENST00000330883.9:c.200A>T	ENSP00000328531.4:p.Lys67Met
ENST00000262186.9:c.1220A>T	ENSP00000262186.5:p.Lys407Met
ENST00000330883.8:c.200A>T	ENSP00000328531.4:p.Lys67Met
ENST00000430723.4:c.872A>T	ENSP00000387657.4:p.Lys291Met
ENST00000461280.1:n.507A>T
ENST00000473610.5:n.525A>T
ENST00000532957.5:n.1443A>T
NM_000238.3:c.1220A>T , LRG_288t1:c.1220A>T	NP_000229.1:p.Lys407Met
NM_001204798.1:c.200A>T	NP_001191727.1:p.Lys67Met
NM_172056.2:c.1220A>T , LRG_288t2:c.1220A>T	NP_742053.1:p.Lys407Met
NM_172057.2:c.200A>T , LRG_288t3:c.200A>T	NP_742054.1:p.Lys67Met
XM_011516185.1:c.920A>T	XP_011514487.1:p.Lys307Met
XM_011516186.1:c.1220A>T	XP_011514488.1:p.Lys407Met
XM_011516185.2:c.920A>T	XP_011514487.1:p.Lys307Met
XM_011516186.3:c.1220A>T	XP_011514488.1:p.Lys407Met
XM_017012195.1:c.1070A>T	XP_016867684.1:p.Lys357Met
XM_017012196.1:c.1043A>T	XP_016867685.1:p.Lys348Met
NM_000238.4:c.1220A>T MANE Select	NP_000229.1:p.Lys407Met
NM_001204798.2:c.200A>T	NP_001191727.1:p.Lys67Met
NM_172057.3:c.200A>T	NP_742054.1:p.Lys67Met