Canonical Allele Identifier: CA1752432093
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150949038T= , CM000669.2:g.150949038T= GRCh38
NC_000007.13:g.150646126T= , CM000669.1:g.150646126T= GRCh37
NC_000007.12:g.150277059T= NCBI36
NG_008916.1:g.33889A= , LRG_288:g.33889A=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.3243A=
ENST00000262186.10:c.2410A= MANE Select ENSP00000262186.5:p.Ile804=
ENST00000330883.9:c.1390A= ENSP00000328531.4:p.Ile464=
ENST00000262186.9:c.2410A= ENSP00000262186.5:p.Ile804=
ENST00000330883.8:c.1390A= ENSP00000328531.4:p.Ile464=
NM_000238.3:c.2410A= , LRG_288t1:c.2410A= NP_000229.1:p.Ile804=
NM_172057.2:c.1390A= , LRG_288t3:c.1390A= NP_742054.1:p.Ile464=
XM_011516185.1:c.2110A= XP_011514487.1:p.Ile704=
XM_011516186.1:c.2410A= XP_011514488.1:p.Ile804=
XM_011516185.2:c.2110A= XP_011514487.1:p.Ile704=
XM_011516186.3:c.2410A= XP_011514488.1:p.Ile804=
XM_017012195.1:c.2260A= XP_016867684.1:p.Ile754=
XM_017012196.1:c.2233A= XP_016867685.1:p.Ile745=
NM_000238.4:c.2410A= MANE Select NP_000229.1:p.Ile804=
NM_172057.3:c.1390A= NP_742054.1:p.Ile464=