Canonical Allele Identifier: CA1752410288
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951661G= , CM000669.2:g.150951661G= GRCh38
NC_000007.13:g.150648749G= , CM000669.1:g.150648749G= GRCh37
NC_000007.12:g.150279682G= NCBI36
NG_008916.1:g.31266C= , LRG_288:g.31266C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1030C=
ENST00000684241.1:n.2565C=
ENST00000262186.10:c.1732C= MANE Select ENSP00000262186.5:p.His578=
ENST00000330883.9:c.712C= ENSP00000328531.4:p.His238=
ENST00000262186.9:c.1732C= ENSP00000262186.5:p.His578=
ENST00000330883.8:c.712C= ENSP00000328531.4:p.His238=
ENST00000430723.4:c.1384C= ENSP00000387657.4:p.His462=
ENST00000461280.1:n.1019C=
ENST00000473610.5:n.1037C=
ENST00000532957.5:n.1955C=
NM_000238.3:c.1732C= , LRG_288t1:c.1732C= NP_000229.1:p.His578=
NM_001204798.1:c.712C= NP_001191727.1:p.His238=
NM_172056.2:c.1732C= , LRG_288t2:c.1732C= NP_742053.1:p.His578=
NM_172057.2:c.712C= , LRG_288t3:c.712C= NP_742054.1:p.His238=
XM_011516185.1:c.1432C= XP_011514487.1:p.His478=
XM_011516186.1:c.1732C= XP_011514488.1:p.His578=
XM_011516185.2:c.1432C= XP_011514487.1:p.His478=
XM_011516186.3:c.1732C= XP_011514488.1:p.His578=
XM_017012195.1:c.1582C= XP_016867684.1:p.His528=
XM_017012196.1:c.1555C= XP_016867685.1:p.His519=
NM_000238.4:c.1732C= MANE Select NP_000229.1:p.His578=
NM_001204798.2:c.712C= NP_001191727.1:p.His238=
NM_172057.3:c.712C= NP_742054.1:p.His238=