Canonical Allele Identifier: CA1752410475
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951712C= , CM000669.2:g.150951712C= GRCh38
NC_000007.13:g.150648800C= , CM000669.1:g.150648800C= GRCh37
NC_000007.12:g.150279733C= NCBI36
NG_008916.1:g.31215G= , LRG_288:g.31215G=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.979G=
ENST00000684241.1:n.2514G=
ENST00000262186.10:c.1681G= MANE Select ENSP00000262186.5:p.Ala561=
ENST00000330883.9:c.661G= ENSP00000328531.4:p.Ala221=
ENST00000262186.9:c.1681G= ENSP00000262186.5:p.Ala561=
ENST00000330883.8:c.661G= ENSP00000328531.4:p.Ala221=
ENST00000430723.4:c.1333G= ENSP00000387657.4:p.Ala445=
ENST00000461280.1:n.968G=
ENST00000473610.5:n.986G=
ENST00000532957.5:n.1904G=
NM_000238.3:c.1681G= , LRG_288t1:c.1681G= NP_000229.1:p.Ala561=
NM_001204798.1:c.661G= NP_001191727.1:p.Ala221=
NM_172056.2:c.1681G= , LRG_288t2:c.1681G= NP_742053.1:p.Ala561=
NM_172057.2:c.661G= , LRG_288t3:c.661G= NP_742054.1:p.Ala221=
XM_011516185.1:c.1381G= XP_011514487.1:p.Ala461=
XM_011516186.1:c.1681G= XP_011514488.1:p.Ala561=
XM_011516185.2:c.1381G= XP_011514487.1:p.Ala461=
XM_011516186.3:c.1681G= XP_011514488.1:p.Ala561=
XM_017012195.1:c.1531G= XP_016867684.1:p.Ala511=
XM_017012196.1:c.1504G= XP_016867685.1:p.Ala502=
NM_000238.4:c.1681G= MANE Select NP_000229.1:p.Ala561=
NM_001204798.2:c.661G= NP_001191727.1:p.Ala221=
NM_172057.3:c.661G= NP_742054.1:p.Ala221=