Canonical Allele Identifier: CA1752409765
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951544A= , CM000669.2:g.150951544A= GRCh38
NC_000007.13:g.150648632A= , CM000669.1:g.150648632A= GRCh37
NC_000007.12:g.150279565A= NCBI36
NG_008916.1:g.31383T= , LRG_288:g.31383T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461280.2:n.1147T=
ENST00000684241.1:n.2682T=
ENST00000262186.10:c.1849T= MANE Select ENSP00000262186.5:p.Phe617=
ENST00000330883.9:c.829T= ENSP00000328531.4:p.Phe277=
ENST00000262186.9:c.1849T= ENSP00000262186.5:p.Phe617=
ENST00000330883.8:c.829T= ENSP00000328531.4:p.Phe277=
ENST00000430723.4:c.1501T= ENSP00000387657.4:p.Phe501=
ENST00000461280.1:n.1136T=
ENST00000473610.5:n.1154T=
ENST00000532957.5:n.2072T=
NM_000238.3:c.1849T= , LRG_288t1:c.1849T= NP_000229.1:p.Phe617=
NM_001204798.1:c.829T= NP_001191727.1:p.Phe277=
NM_172056.2:c.1849T= , LRG_288t2:c.1849T= NP_742053.1:p.Phe617=
NM_172057.2:c.829T= , LRG_288t3:c.829T= NP_742054.1:p.Phe277=
XM_011516185.1:c.1549T= XP_011514487.1:p.Phe517=
XM_011516186.1:c.1849T= XP_011514488.1:p.Phe617=
XM_011516185.2:c.1549T= XP_011514487.1:p.Phe517=
XM_011516186.3:c.1849T= XP_011514488.1:p.Phe617=
XM_017012195.1:c.1699T= XP_016867684.1:p.Phe567=
XM_017012196.1:c.1672T= XP_016867685.1:p.Phe558=
NM_000238.4:c.1849T= MANE Select NP_000229.1:p.Phe617=
NM_001204798.2:c.829T= NP_001191727.1:p.Phe277=
NM_172057.3:c.829T= NP_742054.1:p.Phe277=