Canonical Allele Identifier: CA369863382

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150655524A>T (hg19) ; chr7:g.150958436A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150958436A>T , CM000669.2:g.150958436A>T	GRCh38
NC_000007.13:g.150655524A>T , CM000669.1:g.150655524A>T	GRCh37
NC_000007.12:g.150286457A>T	NCBI36
NG_008916.1:g.24491T>A , LRG_288:g.24491T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684241.1:n.1372T>A
ENST00000262186.10:c.539T>A MANE Select	ENSP00000262186.5:p.Val180Glu
ENST00000262186.9:c.539T>A	ENSP00000262186.5:p.Val180Glu
ENST00000430723.4:c.235-44T>A	ENSP00000387657.4:n.235-44T>A
ENST00000532957.5:n.762T>A
NM_000238.3:c.539T>A , LRG_288t1:c.539T>A	NP_000229.1:p.Val180Glu
NM_172056.2:c.539T>A , LRG_288t2:c.539T>A	NP_742053.1:p.Val180Glu
XM_011516185.1:c.239T>A	XP_011514487.1:p.Val80Glu
XM_011516186.1:c.539T>A	XP_011514488.1:p.Val180Glu
XM_011516185.2:c.239T>A	XP_011514487.1:p.Val80Glu
XM_011516186.3:c.539T>A	XP_011514488.1:p.Val180Glu
XM_017012195.1:c.389T>A	XP_016867684.1:p.Val130Glu
XM_017012196.1:c.362T>A	XP_016867685.1:p.Val121Glu
NM_000238.4:c.539T>A MANE Select	NP_000229.1:p.Val180Glu