Canonical Allele Identifier: CA369856073
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950222T>C , CM000669.2:g.150950222T>C GRCh38
NC_000007.13:g.150647310T>C , CM000669.1:g.150647310T>C GRCh37
NC_000007.12:g.150278243T>C NCBI36
NG_008916.1:g.32705A>G , LRG_288:g.32705A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1642A>G
ENST00000684241.1:n.3177A>G
ENST00000262186.10:c.2344A>G MANE Select ENSP00000262186.5:p.Ile782Val
ENST00000330883.9:c.1324A>G ENSP00000328531.4:p.Ile442Val
ENST00000262186.9:c.2344A>G ENSP00000262186.5:p.Ile782Val
ENST00000330883.8:c.1324A>G ENSP00000328531.4:p.Ile442Val
ENST00000430723.4:c.1996A>G ENSP00000387657.4:p.Ile666Val
ENST00000461280.1:n.1631A>G
ENST00000473610.5:n.1976A>G
ENST00000532957.5:n.2567A>G
NM_000238.3:c.2344A>G , LRG_288t1:c.2344A>G NP_000229.1:p.Ile782Val
NM_001204798.1:c.1324A>G NP_001191727.1:p.Ile442Val
NM_172056.2:c.2344A>G , LRG_288t2:c.2344A>G NP_742053.1:p.Ile782Val
NM_172057.2:c.1324A>G , LRG_288t3:c.1324A>G NP_742054.1:p.Ile442Val
XM_011516185.1:c.2044A>G XP_011514487.1:p.Ile682Val
XM_011516186.1:c.2344A>G XP_011514488.1:p.Ile782Val
XM_011516185.2:c.2044A>G XP_011514487.1:p.Ile682Val
XM_011516186.3:c.2344A>G XP_011514488.1:p.Ile782Val
XM_017012195.1:c.2194A>G XP_016867684.1:p.Ile732Val
XM_017012196.1:c.2167A>G XP_016867685.1:p.Ile723Val
NM_000238.4:c.2344A>G MANE Select NP_000229.1:p.Ile782Val
NM_001204798.2:c.1324A>G NP_001191727.1:p.Ile442Val
NM_172057.3:c.1324A>G NP_742054.1:p.Ile442Val