Canonical Allele Identifier: CA1752434953
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951460T= , CM000669.2:g.150951460T= GRCh38
NC_000007.13:g.150648548T= , CM000669.1:g.150648548T= GRCh37
NC_000007.12:g.150279481T= NCBI36
NG_008916.1:g.31467A= , LRG_288:g.31467A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1231A=
ENST00000683359.1:n.57A=
ENST00000684241.1:n.2766A=
ENST00000262186.10:c.1933A= MANE Select ENSP00000262186.5:p.Met645=
ENST00000330883.9:c.913A= ENSP00000328531.4:p.Met305=
ENST00000262186.9:c.1933A= ENSP00000262186.5:p.Met645=
ENST00000330883.8:c.913A= ENSP00000328531.4:p.Met305=
ENST00000430723.4:c.1585A= ENSP00000387657.4:p.Met529=
ENST00000461280.1:n.1220A=
ENST00000473610.5:n.1238A=
ENST00000532957.5:n.2156A=
NM_000238.3:c.1933A= , LRG_288t1:c.1933A= NP_000229.1:p.Met645=
NM_001204798.1:c.913A= NP_001191727.1:p.Met305=
NM_172056.2:c.1933A= , LRG_288t2:c.1933A= NP_742053.1:p.Met645=
NM_172057.2:c.913A= , LRG_288t3:c.913A= NP_742054.1:p.Met305=
XM_011516185.1:c.1633A= XP_011514487.1:p.Met545=
XM_011516186.1:c.1933A= XP_011514488.1:p.Met645=
XM_011516185.2:c.1633A= XP_011514487.1:p.Met545=
XM_011516186.3:c.1933A= XP_011514488.1:p.Met645=
XM_017012195.1:c.1783A= XP_016867684.1:p.Met595=
XM_017012196.1:c.1756A= XP_016867685.1:p.Met586=
NM_000238.4:c.1933A= MANE Select NP_000229.1:p.Met645=
NM_001204798.2:c.913A= NP_001191727.1:p.Met305=
NM_172057.3:c.913A= NP_742054.1:p.Met305=