Canonical Allele Identifier: CA1752416762
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150957399A= , CM000669.2:g.150957399A= GRCh38
NC_000007.13:g.150654487A= , CM000669.1:g.150654487A= GRCh37
NC_000007.12:g.150285420A= NCBI36
NG_008916.1:g.25528T= , LRG_288:g.25528T=

Transcript Alleles

HGVS Amino-acid change
ENST00000684241.1:n.1853T=
ENST00000262186.10:c.1020T= MANE Select ENSP00000262186.5:p.Phe340=
ENST00000262186.9:c.1020T= ENSP00000262186.5:p.Phe340=
ENST00000430723.4:c.672T= ENSP00000387657.4:p.Phe224=
ENST00000532957.5:n.1243T=
NM_000238.3:c.1020T= , LRG_288t1:c.1020T= NP_000229.1:p.Phe340=
NM_172056.2:c.1020T= , LRG_288t2:c.1020T= NP_742053.1:p.Phe340=
XM_011516185.1:c.720T= XP_011514487.1:p.Phe240=
XM_011516186.1:c.1020T= XP_011514488.1:p.Phe340=
XM_011516185.2:c.720T= XP_011514487.1:p.Phe240=
XM_011516186.3:c.1020T= XP_011514488.1:p.Phe340=
XM_017012195.1:c.870T= XP_016867684.1:p.Phe290=
XM_017012196.1:c.843T= XP_016867685.1:p.Phe281=
NM_000238.4:c.1020T= MANE Select NP_000229.1:p.Phe340=