Canonical Allele Identifier: CA369860195

Gene: KCNH2

Linked Data

• MyVariant Identifiers: chr7:g.150649854A>C (hg19) ; chr7:g.150952766A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150952766A>C , CM000669.2:g.150952766A>C	GRCh38
NC_000007.13:g.150649854A>C , CM000669.1:g.150649854A>C	GRCh37
NC_000007.12:g.150280787A>C	NCBI36
NG_008916.1:g.30161T>G , LRG_288:g.30161T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000461280.2:n.514T>G
ENST00000684116.1:n.109T>G
ENST00000684241.1:n.2049T>G
ENST00000262186.10:c.1216T>G MANE Select	ENSP00000262186.5:p.Phe406Val
ENST00000330883.9:c.196T>G	ENSP00000328531.4:p.Phe66Val
ENST00000262186.9:c.1216T>G	ENSP00000262186.5:p.Phe406Val
ENST00000330883.8:c.196T>G	ENSP00000328531.4:p.Phe66Val
ENST00000430723.4:c.868T>G	ENSP00000387657.4:p.Phe290Val
ENST00000461280.1:n.503T>G
ENST00000473610.5:n.521T>G
ENST00000532957.5:n.1439T>G
NM_000238.3:c.1216T>G , LRG_288t1:c.1216T>G	NP_000229.1:p.Phe406Val
NM_001204798.1:c.196T>G	NP_001191727.1:p.Phe66Val
NM_172056.2:c.1216T>G , LRG_288t2:c.1216T>G	NP_742053.1:p.Phe406Val
NM_172057.2:c.196T>G , LRG_288t3:c.196T>G	NP_742054.1:p.Phe66Val
XM_011516185.1:c.916T>G	XP_011514487.1:p.Phe306Val
XM_011516186.1:c.1216T>G	XP_011514488.1:p.Phe406Val
XM_011516185.2:c.916T>G	XP_011514487.1:p.Phe306Val
XM_011516186.3:c.1216T>G	XP_011514488.1:p.Phe406Val
XM_017012195.1:c.1066T>G	XP_016867684.1:p.Phe356Val
XM_017012196.1:c.1039T>G	XP_016867685.1:p.Phe347Val
NM_000238.4:c.1216T>G MANE Select	NP_000229.1:p.Phe406Val
NM_001204798.2:c.196T>G	NP_001191727.1:p.Phe66Val
NM_172057.3:c.196T>G	NP_742054.1:p.Phe66Val