Canonical Allele Identifier: CA1752409512
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951501G= , CM000669.2:g.150951501G= GRCh38
NC_000007.13:g.150648589G= , CM000669.1:g.150648589G= GRCh37
NC_000007.12:g.150279522G= NCBI36
NG_008916.1:g.31426C= , LRG_288:g.31426C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1190C=
ENST00000683359.1:n.16C=
ENST00000684241.1:n.2725C=
ENST00000262186.10:c.1892C= MANE Select ENSP00000262186.5:p.Ser631=
ENST00000330883.9:c.872C= ENSP00000328531.4:p.Ser291=
ENST00000262186.9:c.1892C= ENSP00000262186.5:p.Ser631=
ENST00000330883.8:c.872C= ENSP00000328531.4:p.Ser291=
ENST00000430723.4:c.1544C= ENSP00000387657.4:p.Ser515=
ENST00000461280.1:n.1179C=
ENST00000473610.5:n.1197C=
ENST00000532957.5:n.2115C=
NM_000238.3:c.1892C= , LRG_288t1:c.1892C= NP_000229.1:p.Ser631=
NM_001204798.1:c.872C= NP_001191727.1:p.Ser291=
NM_172056.2:c.1892C= , LRG_288t2:c.1892C= NP_742053.1:p.Ser631=
NM_172057.2:c.872C= , LRG_288t3:c.872C= NP_742054.1:p.Ser291=
XM_011516185.1:c.1592C= XP_011514487.1:p.Ser531=
XM_011516186.1:c.1892C= XP_011514488.1:p.Ser631=
XM_011516185.2:c.1592C= XP_011514487.1:p.Ser531=
XM_011516186.3:c.1892C= XP_011514488.1:p.Ser631=
XM_017012195.1:c.1742C= XP_016867684.1:p.Ser581=
XM_017012196.1:c.1715C= XP_016867685.1:p.Ser572=
NM_000238.4:c.1892C= MANE Select NP_000229.1:p.Ser631=
NM_001204798.2:c.872C= NP_001191727.1:p.Ser291=
NM_172057.3:c.872C= NP_742054.1:p.Ser291=