Canonical Allele Identifier: CA2695208638
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150958241_150958242dup , CM000669.2:g.150958241_150958242dup GRCh38
NC_000007.13:g.150655329_150655330dup , CM000669.1:g.150655329_150655330dup GRCh37
NC_000007.12:g.150286262_150286263dup NCBI36
NG_008916.1:g.24686_24687dup , LRG_288:g.24686_24687dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.1567_1568dup
ENST00000262186.10:c.734_735dup MANE Select ENSP00000262186.5:p.Gly246ProfsTer?
ENST00000262186.9:c.734_735dup ENSP00000262186.5:p.Gly246ProfsTer?
ENST00000430723.4:c.386_387dup ENSP00000387657.4:p.Gly130ProfsTer?
ENST00000532957.5:n.957_958dup
NM_000238.3:c.734_735dup , LRG_288t1:c.734_735dup NP_000229.1:p.Gly246ProfsTer?
NM_172056.2:c.734_735dup , LRG_288t2:c.734_735dup NP_742053.1:p.Gly246ProfsTer?
XM_011516185.1:c.434_435dup XP_011514487.1:p.Gly146ProfsTer?
XM_011516186.1:c.734_735dup XP_011514488.1:p.Gly246ProfsTer?
XM_011516185.2:c.434_435dup XP_011514487.1:p.Gly146ProfsTer?
XM_011516186.3:c.734_735dup XP_011514488.1:p.Gly246ProfsTer?
XM_017012195.1:c.584_585dup XP_016867684.1:p.Gly196ProfsTer?
XM_017012196.1:c.557_558dup XP_016867685.1:p.Gly187ProfsTer?
NM_000238.4:c.734_735dup MANE Select NP_000229.1:p.Gly246ProfsTer?