Canonical Allele Identifier: CA1752412021
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150952689G= , CM000669.2:g.150952689G= GRCh38
NC_000007.13:g.150649777G= , CM000669.1:g.150649777G= GRCh37
NC_000007.12:g.150280710G= NCBI36
NG_008916.1:g.30238C= , LRG_288:g.30238C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.591C=
ENST00000684116.1:n.186C=
ENST00000684241.1:n.2126C=
ENST00000262186.10:c.1293C= MANE Select ENSP00000262186.5:p.Phe431=
ENST00000330883.9:c.273C= ENSP00000328531.4:p.Phe91=
ENST00000262186.9:c.1293C= ENSP00000262186.5:p.Phe431=
ENST00000330883.8:c.273C= ENSP00000328531.4:p.Phe91=
ENST00000430723.4:c.945C= ENSP00000387657.4:p.Phe315=
ENST00000461280.1:n.580C=
ENST00000473610.5:n.598C=
ENST00000532957.5:n.1516C=
NM_000238.3:c.1293C= , LRG_288t1:c.1293C= NP_000229.1:p.Phe431=
NM_001204798.1:c.273C= NP_001191727.1:p.Phe91=
NM_172056.2:c.1293C= , LRG_288t2:c.1293C= NP_742053.1:p.Phe431=
NM_172057.2:c.273C= , LRG_288t3:c.273C= NP_742054.1:p.Phe91=
XM_011516185.1:c.993C= XP_011514487.1:p.Phe331=
XM_011516186.1:c.1293C= XP_011514488.1:p.Phe431=
XM_011516185.2:c.993C= XP_011514487.1:p.Phe331=
XM_011516186.3:c.1293C= XP_011514488.1:p.Phe431=
XM_017012195.1:c.1143C= XP_016867684.1:p.Phe381=
XM_017012196.1:c.1116C= XP_016867685.1:p.Phe372=
NM_000238.4:c.1293C= MANE Select NP_000229.1:p.Phe431=
NM_001204798.2:c.273C= NP_001191727.1:p.Phe91=
NM_172057.3:c.273C= NP_742054.1:p.Phe91=