Canonical Allele Identifier: CA1752410542
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951743C= , CM000669.2:g.150951743C= GRCh38
NC_000007.13:g.150648831C= , CM000669.1:g.150648831C= GRCh37
NC_000007.12:g.150279764C= NCBI36
NG_008916.1:g.31184G= , LRG_288:g.31184G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461280.2:n.948G=
ENST00000684116.1:n.543G=
ENST00000684241.1:n.2483G=
ENST00000262186.10:c.1650G= MANE Select ENSP00000262186.5:p.Leu550=
ENST00000330883.9:c.630G= ENSP00000328531.4:p.Leu210=
ENST00000262186.9:c.1650G= ENSP00000262186.5:p.Leu550=
ENST00000330883.8:c.630G= ENSP00000328531.4:p.Leu210=
ENST00000430723.4:c.1302G= ENSP00000387657.4:p.Leu434=
ENST00000461280.1:n.937G=
ENST00000473610.5:n.955G=
ENST00000532957.5:n.1873G=
NM_000238.3:c.1650G= , LRG_288t1:c.1650G= NP_000229.1:p.Leu550=
NM_001204798.1:c.630G= NP_001191727.1:p.Leu210=
NM_172056.2:c.1650G= , LRG_288t2:c.1650G= NP_742053.1:p.Leu550=
NM_172057.2:c.630G= , LRG_288t3:c.630G= NP_742054.1:p.Leu210=
XM_011516185.1:c.1350G= XP_011514487.1:p.Leu450=
XM_011516186.1:c.1650G= XP_011514488.1:p.Leu550=
XM_011516185.2:c.1350G= XP_011514487.1:p.Leu450=
XM_011516186.3:c.1650G= XP_011514488.1:p.Leu550=
XM_017012195.1:c.1500G= XP_016867684.1:p.Leu500=
XM_017012196.1:c.1473G= XP_016867685.1:p.Leu491=
NM_000238.4:c.1650G= MANE Select NP_000229.1:p.Leu550=
NM_001204798.2:c.630G= NP_001191727.1:p.Leu210=
NM_172057.3:c.630G= NP_742054.1:p.Leu210=