Canonical Allele Identifier: CA1752412212
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150952774T= , CM000669.2:g.150952774T= GRCh38
NC_000007.13:g.150649862T= , CM000669.1:g.150649862T= GRCh37
NC_000007.12:g.150280795T= NCBI36
NG_008916.1:g.30153A= , LRG_288:g.30153A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.506A=
ENST00000684116.1:n.101A=
ENST00000684241.1:n.2041A=
ENST00000262186.10:c.1208A= MANE Select ENSP00000262186.5:p.Tyr403=
ENST00000330883.9:c.188A= ENSP00000328531.4:p.Tyr63=
ENST00000262186.9:c.1208A= ENSP00000262186.5:p.Tyr403=
ENST00000330883.8:c.188A= ENSP00000328531.4:p.Tyr63=
ENST00000430723.4:c.860A= ENSP00000387657.4:p.Tyr287=
ENST00000461280.1:n.495A=
ENST00000473610.5:n.513A=
ENST00000532957.5:n.1431A=
NM_000238.3:c.1208A= , LRG_288t1:c.1208A= NP_000229.1:p.Tyr403=
NM_001204798.1:c.188A= NP_001191727.1:p.Tyr63=
NM_172056.2:c.1208A= , LRG_288t2:c.1208A= NP_742053.1:p.Tyr403=
NM_172057.2:c.188A= , LRG_288t3:c.188A= NP_742054.1:p.Tyr63=
XM_011516185.1:c.908A= XP_011514487.1:p.Tyr303=
XM_011516186.1:c.1208A= XP_011514488.1:p.Tyr403=
XM_011516185.2:c.908A= XP_011514487.1:p.Tyr303=
XM_011516186.3:c.1208A= XP_011514488.1:p.Tyr403=
XM_017012195.1:c.1058A= XP_016867684.1:p.Tyr353=
XM_017012196.1:c.1031A= XP_016867685.1:p.Tyr344=
NM_000238.4:c.1208A= MANE Select NP_000229.1:p.Tyr403=
NM_001204798.2:c.188A= NP_001191727.1:p.Tyr63=
NM_172057.3:c.188A= NP_742054.1:p.Tyr63=