Canonical Allele Identifier: CA1752432004
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150948980C= , CM000669.2:g.150948980C= GRCh38
NC_000007.13:g.150646068C= , CM000669.1:g.150646068C= GRCh37
NC_000007.12:g.150277001C= NCBI36
NG_008916.1:g.33947G= , LRG_288:g.33947G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.3301G=
ENST00000262186.10:c.2468G= MANE Select ENSP00000262186.5:p.Arg823=
ENST00000330883.9:c.1448G= ENSP00000328531.4:p.Arg483=
ENST00000262186.9:c.2468G= ENSP00000262186.5:p.Arg823=
ENST00000330883.8:c.1448G= ENSP00000328531.4:p.Arg483=
NM_000238.3:c.2468G= , LRG_288t1:c.2468G= NP_000229.1:p.Arg823=
NM_172057.2:c.1448G= , LRG_288t3:c.1448G= NP_742054.1:p.Arg483=
XM_011516185.1:c.2168G= XP_011514487.1:p.Arg723=
XM_011516186.1:c.2468G= XP_011514488.1:p.Arg823=
XM_011516185.2:c.2168G= XP_011514487.1:p.Arg723=
XM_011516186.3:c.2468G= XP_011514488.1:p.Arg823=
XM_017012195.1:c.2318G= XP_016867684.1:p.Arg773=
XM_017012196.1:c.2291G= XP_016867685.1:p.Arg764=
NM_000238.4:c.2468G= MANE Select NP_000229.1:p.Arg823=
NM_172057.3:c.1448G= NP_742054.1:p.Arg483=