Canonical Allele Identifier: CA1752410468
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951711G= , CM000669.2:g.150951711G= GRCh38
NC_000007.13:g.150648799G= , CM000669.1:g.150648799G= GRCh37
NC_000007.12:g.150279732G= NCBI36
NG_008916.1:g.31216C= , LRG_288:g.31216C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.980C=
ENST00000684241.1:n.2515C=
ENST00000262186.10:c.1682C= MANE Select ENSP00000262186.5:p.Ala561=
ENST00000330883.9:c.662C= ENSP00000328531.4:p.Ala221=
ENST00000262186.9:c.1682C= ENSP00000262186.5:p.Ala561=
ENST00000330883.8:c.662C= ENSP00000328531.4:p.Ala221=
ENST00000430723.4:c.1334C= ENSP00000387657.4:p.Ala445=
ENST00000461280.1:n.969C=
ENST00000473610.5:n.987C=
ENST00000532957.5:n.1905C=
NM_000238.3:c.1682C= , LRG_288t1:c.1682C= NP_000229.1:p.Ala561=
NM_001204798.1:c.662C= NP_001191727.1:p.Ala221=
NM_172056.2:c.1682C= , LRG_288t2:c.1682C= NP_742053.1:p.Ala561=
NM_172057.2:c.662C= , LRG_288t3:c.662C= NP_742054.1:p.Ala221=
XM_011516185.1:c.1382C= XP_011514487.1:p.Ala461=
XM_011516186.1:c.1682C= XP_011514488.1:p.Ala561=
XM_011516185.2:c.1382C= XP_011514487.1:p.Ala461=
XM_011516186.3:c.1682C= XP_011514488.1:p.Ala561=
XM_017012195.1:c.1532C= XP_016867684.1:p.Ala511=
XM_017012196.1:c.1505C= XP_016867685.1:p.Ala502=
NM_000238.4:c.1682C= MANE Select NP_000229.1:p.Ala561=
NM_001204798.2:c.662C= NP_001191727.1:p.Ala221=
NM_172057.3:c.662C= NP_742054.1:p.Ala221=