Canonical Allele Identifier: CA1752411560
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150952473C= , CM000669.2:g.150952473C= GRCh38
NC_000007.13:g.150649561C= , CM000669.1:g.150649561C= GRCh37
NC_000007.12:g.150280494C= NCBI36
NG_008916.1:g.30454G= , LRG_288:g.30454G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461280.2:n.807G=
ENST00000684116.1:n.402G=
ENST00000684241.1:n.2342G=
ENST00000262186.10:c.1509G= MANE Select ENSP00000262186.5:p.Val503=
ENST00000330883.9:c.489G= ENSP00000328531.4:p.Val163=
ENST00000262186.9:c.1509G= ENSP00000262186.5:p.Val503=
ENST00000330883.8:c.489G= ENSP00000328531.4:p.Val163=
ENST00000430723.4:c.1161G= ENSP00000387657.4:p.Val387=
ENST00000461280.1:n.796G=
ENST00000473610.5:n.814G=
ENST00000532957.5:n.1732G=
NM_000238.3:c.1509G= , LRG_288t1:c.1509G= NP_000229.1:p.Val503=
NM_001204798.1:c.489G= NP_001191727.1:p.Val163=
NM_172056.2:c.1509G= , LRG_288t2:c.1509G= NP_742053.1:p.Val503=
NM_172057.2:c.489G= , LRG_288t3:c.489G= NP_742054.1:p.Val163=
XM_011516185.1:c.1209G= XP_011514487.1:p.Val403=
XM_011516186.1:c.1509G= XP_011514488.1:p.Val503=
XM_011516185.2:c.1209G= XP_011514487.1:p.Val403=
XM_011516186.3:c.1509G= XP_011514488.1:p.Val503=
XM_017012195.1:c.1359G= XP_016867684.1:p.Val453=
XM_017012196.1:c.1332G= XP_016867685.1:p.Val444=
NM_000238.4:c.1509G= MANE Select NP_000229.1:p.Val503=
NM_001204798.2:c.489G= NP_001191727.1:p.Val163=
NM_172057.3:c.489G= NP_742054.1:p.Val163=