Canonical Allele Identifier: CA1752411891
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150952608G= , CM000669.2:g.150952608G= GRCh38
NC_000007.13:g.150649696G= , CM000669.1:g.150649696G= GRCh37
NC_000007.12:g.150280629G= NCBI36
NG_008916.1:g.30319C= , LRG_288:g.30319C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.672C=
ENST00000684116.1:n.267C=
ENST00000684241.1:n.2207C=
ENST00000262186.10:c.1374C= MANE Select ENSP00000262186.5:p.Ile458=
ENST00000330883.9:c.354C= ENSP00000328531.4:p.Ile118=
ENST00000262186.9:c.1374C= ENSP00000262186.5:p.Ile458=
ENST00000330883.8:c.354C= ENSP00000328531.4:p.Ile118=
ENST00000430723.4:c.1026C= ENSP00000387657.4:p.Ile342=
ENST00000461280.1:n.661C=
ENST00000473610.5:n.679C=
ENST00000532957.5:n.1597C=
NM_000238.3:c.1374C= , LRG_288t1:c.1374C= NP_000229.1:p.Ile458=
NM_001204798.1:c.354C= NP_001191727.1:p.Ile118=
NM_172056.2:c.1374C= , LRG_288t2:c.1374C= NP_742053.1:p.Ile458=
NM_172057.2:c.354C= , LRG_288t3:c.354C= NP_742054.1:p.Ile118=
XM_011516185.1:c.1074C= XP_011514487.1:p.Ile358=
XM_011516186.1:c.1374C= XP_011514488.1:p.Ile458=
XM_011516185.2:c.1074C= XP_011514487.1:p.Ile358=
XM_011516186.3:c.1374C= XP_011514488.1:p.Ile458=
XM_017012195.1:c.1224C= XP_016867684.1:p.Ile408=
XM_017012196.1:c.1197C= XP_016867685.1:p.Ile399=
NM_000238.4:c.1374C= MANE Select NP_000229.1:p.Ile458=
NM_001204798.2:c.354C= NP_001191727.1:p.Ile118=
NM_172057.3:c.354C= NP_742054.1:p.Ile118=