Canonical Allele Identifier: CA007627
Gene: KCNH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 200680
ClinVar RCV Id: RCV000181997
dbSNP Id: rs794728459

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150947667del , CM000669.2:g.150947667del GRCh38
NC_000007.13:g.150644755del , CM000669.1:g.150644755del GRCh37
NC_000007.12:g.150275688del NCBI36
NG_008916.1:g.35262del , LRG_288:g.35262del

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.3739del
ENST00000262186.10:c.2906del MANE Select ENSP00000262186.5:p.Gly969ValfsTer5
ENST00000330883.9:c.1886del ENSP00000328531.4:p.Gly629ValfsTer5
ENST00000262186.9:c.2906del ENSP00000262186.5:p.Gly969ValfsTer5
ENST00000330883.8:c.1886del ENSP00000328531.4:p.Gly629ValfsTer5
NM_000238.3:c.2906del , LRG_288t1:c.2906del NP_000229.1:p.Gly969ValfsTer5
NM_172057.2:c.1886del , LRG_288t3:c.1886del NP_742054.1:p.Gly629ValfsTer5
XM_011516185.1:c.2606del XP_011514487.1:p.Gly869ValfsTer5
XM_011516186.1:c.2719del XP_011514488.1:p.Val907TrpfsTer?
XM_011516185.2:c.2606del XP_011514487.1:p.Gly869ValfsTer5
XM_011516186.3:c.2719del XP_011514488.1:p.Val907TrpfsTer?
XM_017012195.1:c.2756del XP_016867684.1:p.Gly919ValfsTer5
XM_017012196.1:c.2729del XP_016867685.1:p.Gly910ValfsTer5
NM_000238.4:c.2906del MANE Select NP_000229.1:p.Gly969ValfsTer5
NM_172057.3:c.1886del NP_742054.1:p.Gly629ValfsTer5