Canonical Allele Identifier: CA1752409869
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951561T= , CM000669.2:g.150951561T= GRCh38
NC_000007.13:g.150648649T= , CM000669.1:g.150648649T= GRCh37
NC_000007.12:g.150279582T= NCBI36
NG_008916.1:g.31366A= , LRG_288:g.31366A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1130A=
ENST00000684241.1:n.2665A=
ENST00000262186.10:c.1832A= MANE Select ENSP00000262186.5:p.Tyr611=
ENST00000330883.9:c.812A= ENSP00000328531.4:p.Tyr271=
ENST00000262186.9:c.1832A= ENSP00000262186.5:p.Tyr611=
ENST00000330883.8:c.812A= ENSP00000328531.4:p.Tyr271=
ENST00000430723.4:c.1484A= ENSP00000387657.4:p.Tyr495=
ENST00000461280.1:n.1119A=
ENST00000473610.5:n.1137A=
ENST00000532957.5:n.2055A=
NM_000238.3:c.1832A= , LRG_288t1:c.1832A= NP_000229.1:p.Tyr611=
NM_001204798.1:c.812A= NP_001191727.1:p.Tyr271=
NM_172056.2:c.1832A= , LRG_288t2:c.1832A= NP_742053.1:p.Tyr611=
NM_172057.2:c.812A= , LRG_288t3:c.812A= NP_742054.1:p.Tyr271=
XM_011516185.1:c.1532A= XP_011514487.1:p.Tyr511=
XM_011516186.1:c.1832A= XP_011514488.1:p.Tyr611=
XM_011516185.2:c.1532A= XP_011514487.1:p.Tyr511=
XM_011516186.3:c.1832A= XP_011514488.1:p.Tyr611=
XM_017012195.1:c.1682A= XP_016867684.1:p.Tyr561=
XM_017012196.1:c.1655A= XP_016867685.1:p.Tyr552=
NM_000238.4:c.1832A= MANE Select NP_000229.1:p.Tyr611=
NM_001204798.2:c.812A= NP_001191727.1:p.Tyr271=
NM_172057.3:c.812A= NP_742054.1:p.Tyr271=