Canonical Allele Identifier: CA369860168

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649841C>A (hg19) ; chr7:g.150952753C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952753C>A , CM000669.2:g.150952753C>A	GRCh38
NC_000007.13:g.150649841C>A , CM000669.1:g.150649841C>A	GRCh37
NC_000007.12:g.150280774C>A	NCBI36
NG_008916.1:g.30174G>T , LRG_288:g.30174G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.527G>T
ENST00000684116.1:n.122G>T
ENST00000684241.1:n.2062G>T
ENST00000262186.10:c.1229G>T MANE Select	ENSP00000262186.5:p.Trp410Leu
ENST00000330883.9:c.209G>T	ENSP00000328531.4:p.Trp70Leu
ENST00000262186.9:c.1229G>T	ENSP00000262186.5:p.Trp410Leu
ENST00000330883.8:c.209G>T	ENSP00000328531.4:p.Trp70Leu
ENST00000430723.4:c.881G>T	ENSP00000387657.4:p.Trp294Leu
ENST00000461280.1:n.516G>T
ENST00000473610.5:n.534G>T
ENST00000532957.5:n.1452G>T
NM_000238.3:c.1229G>T , LRG_288t1:c.1229G>T	NP_000229.1:p.Trp410Leu
NM_001204798.1:c.209G>T	NP_001191727.1:p.Trp70Leu
NM_172056.2:c.1229G>T , LRG_288t2:c.1229G>T	NP_742053.1:p.Trp410Leu
NM_172057.2:c.209G>T , LRG_288t3:c.209G>T	NP_742054.1:p.Trp70Leu
XM_011516185.1:c.929G>T	XP_011514487.1:p.Trp310Leu
XM_011516186.1:c.1229G>T	XP_011514488.1:p.Trp410Leu
XM_011516185.2:c.929G>T	XP_011514487.1:p.Trp310Leu
XM_011516186.3:c.1229G>T	XP_011514488.1:p.Trp410Leu
XM_017012195.1:c.1079G>T	XP_016867684.1:p.Trp360Leu
XM_017012196.1:c.1052G>T	XP_016867685.1:p.Trp351Leu
NM_000238.4:c.1229G>T MANE Select	NP_000229.1:p.Trp410Leu
NM_001204798.2:c.209G>T	NP_001191727.1:p.Trp70Leu
NM_172057.3:c.209G>T	NP_742054.1:p.Trp70Leu