Canonical Allele Identifier: CA2685607189
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951176_150951181del , CM000669.2:g.150951176_150951181del GRCh38
NC_000007.13:g.150648264_150648269del , CM000669.1:g.150648264_150648269del GRCh37
NC_000007.12:g.150279197_150279202del NCBI36
NG_008916.1:g.31748_31753del , LRG_288:g.31748_31753del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461280.2:n.1244-59_1244-54del
ENST00000683359.1:n.70-59_70-54del
ENST00000684241.1:n.2779-59_2779-54del
ENST00000262186.10:c.1946-59_1946-54del MANE Select ENSP00000262186.5:n.1946-59_1946-54del
ENST00000330883.9:c.926-59_926-54del ENSP00000328531.4:n.926-59_926-54del
ENST00000262186.9:c.1946-59_1946-54del ENSP00000262186.5:n.1946-59_1946-54del
ENST00000330883.8:c.926-59_926-54del ENSP00000328531.4:n.926-59_926-54del
ENST00000430723.4:c.1598-59_1598-54del ENSP00000387657.4:n.1598-59_1598-54del
ENST00000461280.1:n.1233-59_1233-54del
ENST00000473610.5:n.1519_1524del
ENST00000532957.5:n.2169-59_2169-54del
NM_000238.3:c.1946-59_1946-54del , LRG_288t1:c.1946-59_1946-54del NP_000229.1:n.1946-59_1946-54del
NM_001204798.1:c.926-59_926-54del NP_001191727.1:n.926-59_926-54del
NM_172056.2:c.1946-59_1946-54del , LRG_288t2:c.1946-59_1946-54del NP_742053.1:n.1946-59_1946-54del
NM_172057.2:c.926-59_926-54del , LRG_288t3:c.926-59_926-54del NP_742054.1:n.926-59_926-54del
XM_011516185.1:c.1646-59_1646-54del XP_011514487.1:n.1646-59_1646-54del
XM_011516186.1:c.1946-59_1946-54del XP_011514488.1:n.1946-59_1946-54del
XM_011516185.2:c.1646-59_1646-54del XP_011514487.1:n.1646-59_1646-54del
XM_011516186.3:c.1946-59_1946-54del XP_011514488.1:n.1946-59_1946-54del
XM_017012195.1:c.1796-59_1796-54del XP_016867684.1:n.1796-59_1796-54del
XM_017012196.1:c.1769-59_1769-54del XP_016867685.1:n.1769-59_1769-54del
NM_000238.4:c.1946-59_1946-54del MANE Select NP_000229.1:n.1946-59_1946-54del
NM_001204798.2:c.926-59_926-54del NP_001191727.1:n.926-59_926-54del
NM_172057.3:c.926-59_926-54del NP_742054.1:n.926-59_926-54del