Canonical Allele Identifier: CA369857860

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150648570C>A (hg19) ; chr7:g.150951482C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150951482C>A , CM000669.2:g.150951482C>A	GRCh38
NC_000007.13:g.150648570C>A , CM000669.1:g.150648570C>A	GRCh37
NC_000007.12:g.150279503C>A	NCBI36
NG_008916.1:g.31445G>T , LRG_288:g.31445G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461280.2:n.1209G>T
ENST00000683359.1:n.35G>T
ENST00000684241.1:n.2744G>T
ENST00000262186.10:c.1911G>T MANE Select	ENSP00000262186.5:p.Glu637Asp
ENST00000330883.9:c.891G>T	ENSP00000328531.4:p.Glu297Asp
ENST00000262186.9:c.1911G>T	ENSP00000262186.5:p.Glu637Asp
ENST00000330883.8:c.891G>T	ENSP00000328531.4:p.Glu297Asp
ENST00000430723.4:c.1563G>T	ENSP00000387657.4:p.Glu521Asp
ENST00000461280.1:n.1198G>T
ENST00000473610.5:n.1216G>T
ENST00000532957.5:n.2134G>T
NM_000238.3:c.1911G>T , LRG_288t1:c.1911G>T	NP_000229.1:p.Glu637Asp
NM_001204798.1:c.891G>T	NP_001191727.1:p.Glu297Asp
NM_172056.2:c.1911G>T , LRG_288t2:c.1911G>T	NP_742053.1:p.Glu637Asp
NM_172057.2:c.891G>T , LRG_288t3:c.891G>T	NP_742054.1:p.Glu297Asp
XM_011516185.1:c.1611G>T	XP_011514487.1:p.Glu537Asp
XM_011516186.1:c.1911G>T	XP_011514488.1:p.Glu637Asp
XM_011516185.2:c.1611G>T	XP_011514487.1:p.Glu537Asp
XM_011516186.3:c.1911G>T	XP_011514488.1:p.Glu637Asp
XM_017012195.1:c.1761G>T	XP_016867684.1:p.Glu587Asp
XM_017012196.1:c.1734G>T	XP_016867685.1:p.Glu578Asp
NM_000238.4:c.1911G>T MANE Select	NP_000229.1:p.Glu637Asp
NM_001204798.2:c.891G>T	NP_001191727.1:p.Glu297Asp
NM_172057.3:c.891G>T	NP_742054.1:p.Glu297Asp