Canonical Allele Identifier: CA1752434935
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150951455G= , CM000669.2:g.150951455G= GRCh38
NC_000007.13:g.150648543G= , CM000669.1:g.150648543G= GRCh37
NC_000007.12:g.150279476G= NCBI36
NG_008916.1:g.31472C= , LRG_288:g.31472C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1236C=
ENST00000683359.1:n.62C=
ENST00000684241.1:n.2771C=
ENST00000262186.10:c.1938C= MANE Select ENSP00000262186.5:p.Leu646=
ENST00000330883.9:c.918C= ENSP00000328531.4:p.Leu306=
ENST00000262186.9:c.1938C= ENSP00000262186.5:p.Leu646=
ENST00000330883.8:c.918C= ENSP00000328531.4:p.Leu306=
ENST00000430723.4:c.1590C= ENSP00000387657.4:p.Leu530=
ENST00000461280.1:n.1225C=
ENST00000473610.5:n.1243C=
ENST00000532957.5:n.2161C=
NM_000238.3:c.1938C= , LRG_288t1:c.1938C= NP_000229.1:p.Leu646=
NM_001204798.1:c.918C= NP_001191727.1:p.Leu306=
NM_172056.2:c.1938C= , LRG_288t2:c.1938C= NP_742053.1:p.Leu646=
NM_172057.2:c.918C= , LRG_288t3:c.918C= NP_742054.1:p.Leu306=
XM_011516185.1:c.1638C= XP_011514487.1:p.Leu546=
XM_011516186.1:c.1938C= XP_011514488.1:p.Leu646=
XM_011516185.2:c.1638C= XP_011514487.1:p.Leu546=
XM_011516186.3:c.1938C= XP_011514488.1:p.Leu646=
XM_017012195.1:c.1788C= XP_016867684.1:p.Leu596=
XM_017012196.1:c.1761C= XP_016867685.1:p.Leu587=
NM_000238.4:c.1938C= MANE Select NP_000229.1:p.Leu646=
NM_001204798.2:c.918C= NP_001191727.1:p.Leu306=
NM_172057.3:c.918C= NP_742054.1:p.Leu306=