Canonical Allele Identifier: CA1752411924
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150952631G= , CM000669.2:g.150952631G= GRCh38
NC_000007.13:g.150649719G= , CM000669.1:g.150649719G= GRCh37
NC_000007.12:g.150280652G= NCBI36
NG_008916.1:g.30296C= , LRG_288:g.30296C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.649C=
ENST00000684116.1:n.244C=
ENST00000684241.1:n.2184C=
ENST00000262186.10:c.1351C= MANE Select ENSP00000262186.5:p.Pro451=
ENST00000330883.9:c.331C= ENSP00000328531.4:p.Pro111=
ENST00000262186.9:c.1351C= ENSP00000262186.5:p.Pro451=
ENST00000330883.8:c.331C= ENSP00000328531.4:p.Pro111=
ENST00000430723.4:c.1003C= ENSP00000387657.4:p.Pro335=
ENST00000461280.1:n.638C=
ENST00000473610.5:n.656C=
ENST00000532957.5:n.1574C=
NM_000238.3:c.1351C= , LRG_288t1:c.1351C= NP_000229.1:p.Pro451=
NM_001204798.1:c.331C= NP_001191727.1:p.Pro111=
NM_172056.2:c.1351C= , LRG_288t2:c.1351C= NP_742053.1:p.Pro451=
NM_172057.2:c.331C= , LRG_288t3:c.331C= NP_742054.1:p.Pro111=
XM_011516185.1:c.1051C= XP_011514487.1:p.Pro351=
XM_011516186.1:c.1351C= XP_011514488.1:p.Pro451=
XM_011516185.2:c.1051C= XP_011514487.1:p.Pro351=
XM_011516186.3:c.1351C= XP_011514488.1:p.Pro451=
XM_017012195.1:c.1201C= XP_016867684.1:p.Pro401=
XM_017012196.1:c.1174C= XP_016867685.1:p.Pro392=
NM_000238.4:c.1351C= MANE Select NP_000229.1:p.Pro451=
NM_001204798.2:c.331C= NP_001191727.1:p.Pro111=
NM_172057.3:c.331C= NP_742054.1:p.Pro111=