Canonical Allele Identifier: CA1752432024
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948990C= , CM000669.2:g.150948990C= GRCh38
NC_000007.13:g.150646078C= , CM000669.1:g.150646078C= GRCh37
NC_000007.12:g.150277011C= NCBI36
NG_008916.1:g.33937G= , LRG_288:g.33937G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.3291G=
ENST00000262186.10:c.2458G= MANE Select ENSP00000262186.5:p.Gly820=
ENST00000330883.9:c.1438G= ENSP00000328531.4:p.Gly480=
ENST00000262186.9:c.2458G= ENSP00000262186.5:p.Gly820=
ENST00000330883.8:c.1438G= ENSP00000328531.4:p.Gly480=
NM_000238.3:c.2458G= , LRG_288t1:c.2458G= NP_000229.1:p.Gly820=
NM_172057.2:c.1438G= , LRG_288t3:c.1438G= NP_742054.1:p.Gly480=
XM_011516185.1:c.2158G= XP_011514487.1:p.Gly720=
XM_011516186.1:c.2458G= XP_011514488.1:p.Gly820=
XM_011516185.2:c.2158G= XP_011514487.1:p.Gly720=
XM_011516186.3:c.2458G= XP_011514488.1:p.Gly820=
XM_017012195.1:c.2308G= XP_016867684.1:p.Gly770=
XM_017012196.1:c.2281G= XP_016867685.1:p.Gly761=
NM_000238.4:c.2458G= MANE Select NP_000229.1:p.Gly820=
NM_172057.3:c.1438G= NP_742054.1:p.Gly480=