Canonical Allele Identifier: CA1752441835
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150975021_150975025delinsTCACA , CM000669.2:g.150975021_150975025delinsTCACA GRCh38
NC_000007.13:g.150672109_150672113delinsTCACA , CM000669.1:g.150672109_150672113delinsTCACA GRCh37
NC_000007.12:g.150303042_150303046delinsTCACA NCBI36
NG_008916.1:g.7902_7906delinsTGTGA , LRG_288:g.7902_7906delinsTGTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000262186.10:c.77-84_77-80delinsTGTGA MANE Select ENSP00000262186.5:n.77-84_77-80delinsTGTGA
ENST00000262186.9:c.77-84_77-80delinsTGTGA ENSP00000262186.5:n.77-84_77-80delinsTGTGA
ENST00000430723.4:c.-101-84_-101-80delinsTGTGA ENSP00000387657.4:n.-101-84_-101-80delinsTGTGA
ENST00000532957.5:n.300-84_300-80delinsTGTGA
NM_000238.3:c.77-84_77-80delinsTGTGA , LRG_288t1:c.77-84_77-80delinsTGTGA NP_000229.1:n.77-84_77-80delinsTGTGA
NM_172056.2:c.77-84_77-80delinsTGTGA , LRG_288t2:c.77-84_77-80delinsTGTGA NP_742053.1:n.77-84_77-80delinsTGTGA
XM_011516186.1:c.77-84_77-80delinsTGTGA XP_011514488.1:n.77-84_77-80delinsTGTGA
XM_011516186.3:c.77-84_77-80delinsTGTGA XP_011514488.1:n.77-84_77-80delinsTGTGA
XM_017012196.1:c.-102_-102+4delinsTGTGA
NM_000238.4:c.77-84_77-80delinsTGTGA MANE Select NP_000229.1:n.77-84_77-80delinsTGTGA