Canonical Allele Identifier: CA005840
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 67313
dbSNP Id: rs199472956

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951508T>C , CM000669.2:g.150951508T>C GRCh38
NC_000007.13:g.150648596T>C , CM000669.1:g.150648596T>C GRCh37
NC_000007.12:g.150279529T>C NCBI36
NG_008916.1:g.31419A>G , LRG_288:g.31419A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1183A>G
ENST00000683359.1:n.9A>G
ENST00000684241.1:n.2718A>G
ENST00000262186.10:c.1885A>G MANE Select ENSP00000262186.5:p.Asn629Asp
ENST00000330883.9:c.865A>G ENSP00000328531.4:p.Asn289Asp
ENST00000262186.9:c.1885A>G ENSP00000262186.5:p.Asn629Asp
ENST00000330883.8:c.865A>G ENSP00000328531.4:p.Asn289Asp
ENST00000430723.4:c.1537A>G ENSP00000387657.4:p.Asn513Asp
ENST00000461280.1:n.1172A>G
ENST00000473610.5:n.1190A>G
ENST00000532957.5:n.2108A>G
NM_000238.3:c.1885A>G , LRG_288t1:c.1885A>G NP_000229.1:p.Asn629Asp
NM_001204798.1:c.865A>G NP_001191727.1:p.Asn289Asp
NM_172056.2:c.1885A>G , LRG_288t2:c.1885A>G NP_742053.1:p.Asn629Asp
NM_172057.2:c.865A>G , LRG_288t3:c.865A>G NP_742054.1:p.Asn289Asp
XM_011516185.1:c.1585A>G XP_011514487.1:p.Asn529Asp
XM_011516186.1:c.1885A>G XP_011514488.1:p.Asn629Asp
XM_011516185.2:c.1585A>G XP_011514487.1:p.Asn529Asp
XM_011516186.3:c.1885A>G XP_011514488.1:p.Asn629Asp
XM_017012195.1:c.1735A>G XP_016867684.1:p.Asn579Asp
XM_017012196.1:c.1708A>G XP_016867685.1:p.Asn570Asp
NM_000238.4:c.1885A>G MANE Select NP_000229.1:p.Asn629Asp
NM_001204798.2:c.865A>G NP_001191727.1:p.Asn289Asp
NM_172057.3:c.865A>G NP_742054.1:p.Asn289Asp