Canonical Allele Identifier: CA458871375
Gene: KCNH2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.150647500C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950412C>T , CM000669.2:g.150950412C>T GRCh38
NC_000007.13:g.150647500C>T , CM000669.1:g.150647500C>T GRCh37
NC_000007.12:g.150278433C>T NCBI36
NG_008916.1:g.32515G>A , LRG_288:g.32515G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000461280.2:n.1452G>A
ENST00000684241.1:n.2987G>A
ENST00000262186.10:c.2154G>A MANE Select ENSP00000262186.5:p.Lys718=
ENST00000330883.9:c.1134G>A ENSP00000328531.4:p.Lys378=
ENST00000262186.9:c.2154G>A ENSP00000262186.5:p.Lys718=
ENST00000330883.8:c.1134G>A ENSP00000328531.4:p.Lys378=
ENST00000430723.4:c.1806G>A ENSP00000387657.4:p.Lys602=
ENST00000461280.1:n.1441G>A
ENST00000473610.5:n.1786G>A
ENST00000532957.5:n.2377G>A
NM_000238.3:c.2154G>A , LRG_288t1:c.2154G>A NP_000229.1:p.Lys718=
NM_001204798.1:c.1134G>A NP_001191727.1:p.Lys378=
NM_172056.2:c.2154G>A , LRG_288t2:c.2154G>A NP_742053.1:p.Lys718=
NM_172057.2:c.1134G>A , LRG_288t3:c.1134G>A NP_742054.1:p.Lys378=
XM_011516185.1:c.1854G>A XP_011514487.1:p.Lys618=
XM_011516186.1:c.2154G>A XP_011514488.1:p.Lys718=
XM_011516185.2:c.1854G>A XP_011514487.1:p.Lys618=
XM_011516186.3:c.2154G>A XP_011514488.1:p.Lys718=
XM_017012195.1:c.2004G>A XP_016867684.1:p.Lys668=
XM_017012196.1:c.1977G>A XP_016867685.1:p.Lys659=
NM_000238.4:c.2154G>A MANE Select NP_000229.1:p.Lys718=
NM_001204798.2:c.1134G>A NP_001191727.1:p.Lys378=
NM_172057.3:c.1134G>A NP_742054.1:p.Lys378=