Canonical Allele Identifier: CA305342
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 200717
dbSNP Id: rs794728476

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150974773_150974781dup , CM000669.2:g.150974773_150974781dup GRCh38
NC_000007.13:g.150671861_150671869dup , CM000669.1:g.150671861_150671869dup GRCh37
NC_000007.12:g.150302794_150302802dup NCBI36
NG_008916.1:g.8153_8161dup , LRG_288:g.8153_8161dup

Transcript Alleles

HGVS Amino-acid change
ENST00000262186.10:c.244_252dup MANE Select ENSP00000262186.5:p.Gln84_Ala85insIleAlaG...
ENST00000262186.9:c.244_252dup ENSP00000262186.5:p.Gln84_Ala85insIleAlaG...
ENST00000430723.4:c.67_75dup ENSP00000387657.4:p.Gln25_Ala26insIleAlaG...
ENST00000532957.5:n.467_475dup
NM_000238.3:c.244_252dup , LRG_288t1:c.244_252dup NP_000229.1:p.Gln84_Ala85insIleAlaGln
NM_172056.2:c.244_252dup , LRG_288t2:c.244_252dup NP_742053.1:p.Gln84_Ala85insIleAlaGln
XM_011516186.1:c.244_252dup XP_011514488.1:p.Gln84_Ala85insIleAlaGln
XM_011516186.3:c.244_252dup XP_011514488.1:p.Gln84_Ala85insIleAlaGln
XM_017012196.1:c.67_75dup XP_016867685.1:p.Gln25_Ala26insIleAlaGln
NM_000238.4:c.244_252dup MANE Select NP_000229.1:p.Gln84_Ala85insIleAlaGln