Canonical Allele Identifier: CA1752412017
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150952678T= , CM000669.2:g.150952678T= GRCh38
NC_000007.13:g.150649766T= , CM000669.1:g.150649766T= GRCh37
NC_000007.12:g.150280699T= NCBI36
NG_008916.1:g.30249A= , LRG_288:g.30249A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.602A=
ENST00000684116.1:n.197A=
ENST00000684241.1:n.2137A=
ENST00000262186.10:c.1304A= MANE Select ENSP00000262186.5:p.Glu435=
ENST00000330883.9:c.284A= ENSP00000328531.4:p.Glu95=
ENST00000262186.9:c.1304A= ENSP00000262186.5:p.Glu435=
ENST00000330883.8:c.284A= ENSP00000328531.4:p.Glu95=
ENST00000430723.4:c.956A= ENSP00000387657.4:p.Glu319=
ENST00000461280.1:n.591A=
ENST00000473610.5:n.609A=
ENST00000532957.5:n.1527A=
NM_000238.3:c.1304A= , LRG_288t1:c.1304A= NP_000229.1:p.Glu435=
NM_001204798.1:c.284A= NP_001191727.1:p.Glu95=
NM_172056.2:c.1304A= , LRG_288t2:c.1304A= NP_742053.1:p.Glu435=
NM_172057.2:c.284A= , LRG_288t3:c.284A= NP_742054.1:p.Glu95=
XM_011516185.1:c.1004A= XP_011514487.1:p.Glu335=
XM_011516186.1:c.1304A= XP_011514488.1:p.Glu435=
XM_011516185.2:c.1004A= XP_011514487.1:p.Glu335=
XM_011516186.3:c.1304A= XP_011514488.1:p.Glu435=
XM_017012195.1:c.1154A= XP_016867684.1:p.Glu385=
XM_017012196.1:c.1127A= XP_016867685.1:p.Glu376=
NM_000238.4:c.1304A= MANE Select NP_000229.1:p.Glu435=
NM_001204798.2:c.284A= NP_001191727.1:p.Glu95=
NM_172057.3:c.284A= NP_742054.1:p.Glu95=