Canonical Allele Identifier: CA1752409664
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951523T= , CM000669.2:g.150951523T= GRCh38
NC_000007.13:g.150648611T= , CM000669.1:g.150648611T= GRCh37
NC_000007.12:g.150279544T= NCBI36
NG_008916.1:g.31404A= , LRG_288:g.31404A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1168A=
ENST00000684241.1:n.2703A=
ENST00000262186.10:c.1870A= MANE Select ENSP00000262186.5:p.Ser624=
ENST00000330883.9:c.850A= ENSP00000328531.4:p.Ser284=
ENST00000262186.9:c.1870A= ENSP00000262186.5:p.Ser624=
ENST00000330883.8:c.850A= ENSP00000328531.4:p.Ser284=
ENST00000430723.4:c.1522A= ENSP00000387657.4:p.Ser508=
ENST00000461280.1:n.1157A=
ENST00000473610.5:n.1175A=
ENST00000532957.5:n.2093A=
NM_000238.3:c.1870A= , LRG_288t1:c.1870A= NP_000229.1:p.Ser624=
NM_001204798.1:c.850A= NP_001191727.1:p.Ser284=
NM_172056.2:c.1870A= , LRG_288t2:c.1870A= NP_742053.1:p.Ser624=
NM_172057.2:c.850A= , LRG_288t3:c.850A= NP_742054.1:p.Ser284=
XM_011516185.1:c.1570A= XP_011514487.1:p.Ser524=
XM_011516186.1:c.1870A= XP_011514488.1:p.Ser624=
XM_011516185.2:c.1570A= XP_011514487.1:p.Ser524=
XM_011516186.3:c.1870A= XP_011514488.1:p.Ser624=
XM_017012195.1:c.1720A= XP_016867684.1:p.Ser574=
XM_017012196.1:c.1693A= XP_016867685.1:p.Ser565=
NM_000238.4:c.1870A= MANE Select NP_000229.1:p.Ser624=
NM_001204798.2:c.850A= NP_001191727.1:p.Ser284=
NM_172057.3:c.850A= NP_742054.1:p.Ser284=