Canonical Allele Identifier: CA2685605137
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150950489_150950499del , CM000669.2:g.150950489_150950499del GRCh38
NC_000007.13:g.150647577_150647587del , CM000669.1:g.150647577_150647587del GRCh37
NC_000007.12:g.150278510_150278520del NCBI36
NG_008916.1:g.32429_32439del , LRG_288:g.32429_32439del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461280.2:n.1444-78_1444-68del
ENST00000684241.1:n.2979-78_2979-68del
ENST00000262186.10:c.2146-78_2146-68del MANE Select ENSP00000262186.5:n.2146-78_2146-68del
ENST00000330883.9:c.1126-78_1126-68del ENSP00000328531.4:n.1126-78_1126-68del
ENST00000262186.9:c.2146-78_2146-68del ENSP00000262186.5:n.2146-78_2146-68del
ENST00000330883.8:c.1126-78_1126-68del ENSP00000328531.4:n.1126-78_1126-68del
ENST00000430723.4:c.1798-78_1798-68del ENSP00000387657.4:n.1798-78_1798-68del
ENST00000461280.1:n.1433-78_1433-68del
ENST00000473610.5:n.1778-78_1778-68del
ENST00000532957.5:n.2369-78_2369-68del
NM_000238.3:c.2146-78_2146-68del , LRG_288t1:c.2146-78_2146-68del NP_000229.1:n.2146-78_2146-68del
NM_001204798.1:c.1126-78_1126-68del NP_001191727.1:n.1126-78_1126-68del
NM_172056.2:c.2146-78_2146-68del , LRG_288t2:c.2146-78_2146-68del NP_742053.1:n.2146-78_2146-68del
NM_172057.2:c.1126-78_1126-68del , LRG_288t3:c.1126-78_1126-68del NP_742054.1:n.1126-78_1126-68del
XM_011516185.1:c.1846-78_1846-68del XP_011514487.1:n.1846-78_1846-68del
XM_011516186.1:c.2146-78_2146-68del XP_011514488.1:n.2146-78_2146-68del
XM_011516185.2:c.1846-78_1846-68del XP_011514487.1:n.1846-78_1846-68del
XM_011516186.3:c.2146-78_2146-68del XP_011514488.1:n.2146-78_2146-68del
XM_017012195.1:c.1996-78_1996-68del XP_016867684.1:n.1996-78_1996-68del
XM_017012196.1:c.1969-78_1969-68del XP_016867685.1:n.1969-78_1969-68del
NM_000238.4:c.2146-78_2146-68del MANE Select NP_000229.1:n.2146-78_2146-68del
NM_001204798.2:c.1126-78_1126-68del NP_001191727.1:n.1126-78_1126-68del
NM_172057.3:c.1126-78_1126-68del NP_742054.1:n.1126-78_1126-68del