Canonical Allele Identifier: CA1752410263
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951647G= , CM000669.2:g.150951647G= GRCh38
NC_000007.13:g.150648735G= , CM000669.1:g.150648735G= GRCh37
NC_000007.12:g.150279668G= NCBI36
NG_008916.1:g.31280C= , LRG_288:g.31280C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1044C=
ENST00000684241.1:n.2579C=
ENST00000262186.10:c.1746C= MANE Select ENSP00000262186.5:p.Arg582=
ENST00000330883.9:c.726C= ENSP00000328531.4:p.Arg242=
ENST00000262186.9:c.1746C= ENSP00000262186.5:p.Arg582=
ENST00000330883.8:c.726C= ENSP00000328531.4:p.Arg242=
ENST00000430723.4:c.1398C= ENSP00000387657.4:p.Arg466=
ENST00000461280.1:n.1033C=
ENST00000473610.5:n.1051C=
ENST00000532957.5:n.1969C=
NM_000238.3:c.1746C= , LRG_288t1:c.1746C= NP_000229.1:p.Arg582=
NM_001204798.1:c.726C= NP_001191727.1:p.Arg242=
NM_172056.2:c.1746C= , LRG_288t2:c.1746C= NP_742053.1:p.Arg582=
NM_172057.2:c.726C= , LRG_288t3:c.726C= NP_742054.1:p.Arg242=
XM_011516185.1:c.1446C= XP_011514487.1:p.Arg482=
XM_011516186.1:c.1746C= XP_011514488.1:p.Arg582=
XM_011516185.2:c.1446C= XP_011514487.1:p.Arg482=
XM_011516186.3:c.1746C= XP_011514488.1:p.Arg582=
XM_017012195.1:c.1596C= XP_016867684.1:p.Arg532=
XM_017012196.1:c.1569C= XP_016867685.1:p.Arg523=
NM_000238.4:c.1746C= MANE Select NP_000229.1:p.Arg582=
NM_001204798.2:c.726C= NP_001191727.1:p.Arg242=
NM_172057.3:c.726C= NP_742054.1:p.Arg242=