Canonical Allele Identifier: CA369855989
Gene: KCNH2 HGNC NCBI

Linked Data

dbSNP Id: rs2116948427

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950173A>G , CM000669.2:g.150950173A>G GRCh38
NC_000007.13:g.150647261A>G , CM000669.1:g.150647261A>G GRCh37
NC_000007.12:g.150278194A>G NCBI36
NG_008916.1:g.32754T>C , LRG_288:g.32754T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000461280.2:n.1691T>C
ENST00000684241.1:n.3226T>C
ENST00000262186.10:c.2393T>C MANE Select ENSP00000262186.5:p.Ile798Thr
ENST00000330883.9:c.1373T>C ENSP00000328531.4:p.Ile458Thr
ENST00000262186.9:c.2393T>C ENSP00000262186.5:p.Ile798Thr
ENST00000330883.8:c.1373T>C ENSP00000328531.4:p.Ile458Thr
ENST00000430723.4:c.2045T>C ENSP00000387657.4:p.Ile682Thr
ENST00000461280.1:n.1680T>C
ENST00000473610.5:n.2025T>C
ENST00000532957.5:n.2616T>C
NM_000238.3:c.2393T>C , LRG_288t1:c.2393T>C NP_000229.1:p.Ile798Thr
NM_001204798.1:c.1373T>C NP_001191727.1:p.Ile458Thr
NM_172056.2:c.2393T>C , LRG_288t2:c.2393T>C NP_742053.1:p.Ile798Thr
NM_172057.2:c.1373T>C , LRG_288t3:c.1373T>C NP_742054.1:p.Ile458Thr
XM_011516185.1:c.2093T>C XP_011514487.1:p.Ile698Thr
XM_011516186.1:c.2393T>C XP_011514488.1:p.Ile798Thr
XM_011516185.2:c.2093T>C XP_011514487.1:p.Ile698Thr
XM_011516186.3:c.2393T>C XP_011514488.1:p.Ile798Thr
XM_017012195.1:c.2243T>C XP_016867684.1:p.Ile748Thr
XM_017012196.1:c.2216T>C XP_016867685.1:p.Ile739Thr
NM_000238.4:c.2393T>C MANE Select NP_000229.1:p.Ile798Thr
NM_001204798.2:c.1373T>C NP_001191727.1:p.Ile458Thr
NM_172057.3:c.1373T>C NP_742054.1:p.Ile458Thr