Canonical Allele Identifier: CA1752434926
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951450C= , CM000669.2:g.150951450C= GRCh38
NC_000007.13:g.150648538C= , CM000669.1:g.150648538C= GRCh37
NC_000007.12:g.150279471C= NCBI36
NG_008916.1:g.31477G= , LRG_288:g.31477G=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1241G=
ENST00000683359.1:n.67G=
ENST00000684241.1:n.2776G=
ENST00000262186.10:c.1943G= MANE Select ENSP00000262186.5:p.Gly648=
ENST00000330883.9:c.923G= ENSP00000328531.4:p.Gly308=
ENST00000262186.9:c.1943G= ENSP00000262186.5:p.Gly648=
ENST00000330883.8:c.923G= ENSP00000328531.4:p.Gly308=
ENST00000430723.4:c.1595G= ENSP00000387657.4:p.Gly532=
ENST00000461280.1:n.1230G=
ENST00000473610.5:n.1248G=
ENST00000532957.5:n.2166G=
NM_000238.3:c.1943G= , LRG_288t1:c.1943G= NP_000229.1:p.Gly648=
NM_001204798.1:c.923G= NP_001191727.1:p.Gly308=
NM_172056.2:c.1943G= , LRG_288t2:c.1943G= NP_742053.1:p.Gly648=
NM_172057.2:c.923G= , LRG_288t3:c.923G= NP_742054.1:p.Gly308=
XM_011516185.1:c.1643G= XP_011514487.1:p.Gly548=
XM_011516186.1:c.1943G= XP_011514488.1:p.Gly648=
XM_011516185.2:c.1643G= XP_011514487.1:p.Gly548=
XM_011516186.3:c.1943G= XP_011514488.1:p.Gly648=
XM_017012195.1:c.1793G= XP_016867684.1:p.Gly598=
XM_017012196.1:c.1766G= XP_016867685.1:p.Gly589=
NM_000238.4:c.1943G= MANE Select NP_000229.1:p.Gly648=
NM_001204798.2:c.923G= NP_001191727.1:p.Gly308=
NM_172057.3:c.923G= NP_742054.1:p.Gly308=