Canonical Allele Identifier: CA2685605034
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950481_150950485del , CM000669.2:g.150950481_150950485del GRCh38
NC_000007.13:g.150647569_150647573del , CM000669.1:g.150647569_150647573del GRCh37
NC_000007.12:g.150278502_150278506del NCBI36
NG_008916.1:g.32446_32450del , LRG_288:g.32446_32450del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461280.2:n.1444-61_1444-57del
ENST00000684241.1:n.2979-61_2979-57del
ENST00000262186.10:c.2146-61_2146-57del MANE Select ENSP00000262186.5:n.2146-61_2146-57del
ENST00000330883.9:c.1126-61_1126-57del ENSP00000328531.4:n.1126-61_1126-57del
ENST00000262186.9:c.2146-61_2146-57del ENSP00000262186.5:n.2146-61_2146-57del
ENST00000330883.8:c.1126-61_1126-57del ENSP00000328531.4:n.1126-61_1126-57del
ENST00000430723.4:c.1798-61_1798-57del ENSP00000387657.4:n.1798-61_1798-57del
ENST00000461280.1:n.1433-61_1433-57del
ENST00000473610.5:n.1778-61_1778-57del
ENST00000532957.5:n.2369-61_2369-57del
NM_000238.3:c.2146-61_2146-57del , LRG_288t1:c.2146-61_2146-57del NP_000229.1:n.2146-61_2146-57del
NM_001204798.1:c.1126-61_1126-57del NP_001191727.1:n.1126-61_1126-57del
NM_172056.2:c.2146-61_2146-57del , LRG_288t2:c.2146-61_2146-57del NP_742053.1:n.2146-61_2146-57del
NM_172057.2:c.1126-61_1126-57del , LRG_288t3:c.1126-61_1126-57del NP_742054.1:n.1126-61_1126-57del
XM_011516185.1:c.1846-61_1846-57del XP_011514487.1:n.1846-61_1846-57del
XM_011516186.1:c.2146-61_2146-57del XP_011514488.1:n.2146-61_2146-57del
XM_011516185.2:c.1846-61_1846-57del XP_011514487.1:n.1846-61_1846-57del
XM_011516186.3:c.2146-61_2146-57del XP_011514488.1:n.2146-61_2146-57del
XM_017012195.1:c.1996-61_1996-57del XP_016867684.1:n.1996-61_1996-57del
XM_017012196.1:c.1969-61_1969-57del XP_016867685.1:n.1969-61_1969-57del
NM_000238.4:c.2146-61_2146-57del MANE Select NP_000229.1:n.2146-61_2146-57del
NM_001204798.2:c.1126-61_1126-57del NP_001191727.1:n.1126-61_1126-57del
NM_172057.3:c.1126-61_1126-57del NP_742054.1:n.1126-61_1126-57del