Canonical Allele Identifier: CA1752412088
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150952707T= , CM000669.2:g.150952707T= GRCh38
NC_000007.13:g.150649795T= , CM000669.1:g.150649795T= GRCh37
NC_000007.12:g.150280728T= NCBI36
NG_008916.1:g.30220A= , LRG_288:g.30220A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.573A=
ENST00000684116.1:n.168A=
ENST00000684241.1:n.2108A=
ENST00000262186.10:c.1275A= MANE Select ENSP00000262186.5:p.Thr425=
ENST00000330883.9:c.255A= ENSP00000328531.4:p.Thr85=
ENST00000262186.9:c.1275A= ENSP00000262186.5:p.Thr425=
ENST00000330883.8:c.255A= ENSP00000328531.4:p.Thr85=
ENST00000430723.4:c.927A= ENSP00000387657.4:p.Thr309=
ENST00000461280.1:n.562A=
ENST00000473610.5:n.580A=
ENST00000532957.5:n.1498A=
NM_000238.3:c.1275A= , LRG_288t1:c.1275A= NP_000229.1:p.Thr425=
NM_001204798.1:c.255A= NP_001191727.1:p.Thr85=
NM_172056.2:c.1275A= , LRG_288t2:c.1275A= NP_742053.1:p.Thr425=
NM_172057.2:c.255A= , LRG_288t3:c.255A= NP_742054.1:p.Thr85=
XM_011516185.1:c.975A= XP_011514487.1:p.Thr325=
XM_011516186.1:c.1275A= XP_011514488.1:p.Thr425=
XM_011516185.2:c.975A= XP_011514487.1:p.Thr325=
XM_011516186.3:c.1275A= XP_011514488.1:p.Thr425=
XM_017012195.1:c.1125A= XP_016867684.1:p.Thr375=
XM_017012196.1:c.1098A= XP_016867685.1:p.Thr366=
NM_000238.4:c.1275A= MANE Select NP_000229.1:p.Thr425=
NM_001204798.2:c.255A= NP_001191727.1:p.Thr85=
NM_172057.3:c.255A= NP_742054.1:p.Thr85=