Canonical Allele Identifier: CA369856464
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950323T>A , CM000669.2:g.150950323T>A GRCh38
NC_000007.13:g.150647411T>A , CM000669.1:g.150647411T>A GRCh37
NC_000007.12:g.150278344T>A NCBI36
NG_008916.1:g.32604A>T , LRG_288:g.32604A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000461280.2:n.1541A>T
ENST00000684241.1:n.3076A>T
ENST00000262186.10:c.2243A>T MANE Select ENSP00000262186.5:p.Lys748Met
ENST00000330883.9:c.1223A>T ENSP00000328531.4:p.Lys408Met
ENST00000262186.9:c.2243A>T ENSP00000262186.5:p.Lys748Met
ENST00000330883.8:c.1223A>T ENSP00000328531.4:p.Lys408Met
ENST00000430723.4:c.1895A>T ENSP00000387657.4:p.Lys632Met
ENST00000461280.1:n.1530A>T
ENST00000473610.5:n.1875A>T
ENST00000532957.5:n.2466A>T
NM_000238.3:c.2243A>T , LRG_288t1:c.2243A>T NP_000229.1:p.Lys748Met
NM_001204798.1:c.1223A>T NP_001191727.1:p.Lys408Met
NM_172056.2:c.2243A>T , LRG_288t2:c.2243A>T NP_742053.1:p.Lys748Met
NM_172057.2:c.1223A>T , LRG_288t3:c.1223A>T NP_742054.1:p.Lys408Met
XM_011516185.1:c.1943A>T XP_011514487.1:p.Lys648Met
XM_011516186.1:c.2243A>T XP_011514488.1:p.Lys748Met
XM_011516185.2:c.1943A>T XP_011514487.1:p.Lys648Met
XM_011516186.3:c.2243A>T XP_011514488.1:p.Lys748Met
XM_017012195.1:c.2093A>T XP_016867684.1:p.Lys698Met
XM_017012196.1:c.2066A>T XP_016867685.1:p.Lys689Met
NM_000238.4:c.2243A>T MANE Select NP_000229.1:p.Lys748Met
NM_001204798.2:c.1223A>T NP_001191727.1:p.Lys408Met
NM_172057.3:c.1223A>T NP_742054.1:p.Lys408Met