Canonical Allele Identifier: CA1752433564
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950325G= , CM000669.2:g.150950325G= GRCh38
NC_000007.13:g.150647413G= , CM000669.1:g.150647413G= GRCh37
NC_000007.12:g.150278346G= NCBI36
NG_008916.1:g.32602C= , LRG_288:g.32602C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461280.2:n.1539C=
ENST00000684241.1:n.3074C=
ENST00000262186.10:c.2241C= MANE Select ENSP00000262186.5:p.Thr747=
ENST00000330883.9:c.1221C= ENSP00000328531.4:p.Thr407=
ENST00000262186.9:c.2241C= ENSP00000262186.5:p.Thr747=
ENST00000330883.8:c.1221C= ENSP00000328531.4:p.Thr407=
ENST00000430723.4:c.1893C= ENSP00000387657.4:p.Thr631=
ENST00000461280.1:n.1528C=
ENST00000473610.5:n.1873C=
ENST00000532957.5:n.2464C=
NM_000238.3:c.2241C= , LRG_288t1:c.2241C= NP_000229.1:p.Thr747=
NM_001204798.1:c.1221C= NP_001191727.1:p.Thr407=
NM_172056.2:c.2241C= , LRG_288t2:c.2241C= NP_742053.1:p.Thr747=
NM_172057.2:c.1221C= , LRG_288t3:c.1221C= NP_742054.1:p.Thr407=
XM_011516185.1:c.1941C= XP_011514487.1:p.Thr647=
XM_011516186.1:c.2241C= XP_011514488.1:p.Thr747=
XM_011516185.2:c.1941C= XP_011514487.1:p.Thr647=
XM_011516186.3:c.2241C= XP_011514488.1:p.Thr747=
XM_017012195.1:c.2091C= XP_016867684.1:p.Thr697=
XM_017012196.1:c.2064C= XP_016867685.1:p.Thr688=
NM_000238.4:c.2241C= MANE Select NP_000229.1:p.Thr747=
NM_001204798.2:c.1221C= NP_001191727.1:p.Thr407=
NM_172057.3:c.1221C= NP_742054.1:p.Thr407=