Canonical Allele Identifier: CA2685602181
Gene: KCNH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150947925_150947929del , CM000669.2:g.150947925_150947929del GRCh38
NC_000007.13:g.150645013_150645017del , CM000669.1:g.150645013_150645017del GRCh37
NC_000007.12:g.150275946_150275950del NCBI36
NG_008916.1:g.35001_35005del , LRG_288:g.35001_35005del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.3526-48_3526-44del
ENST00000262186.10:c.2693-48_2693-44del MANE Select ENSP00000262186.5:n.2693-48_2693-44del
ENST00000330883.9:c.1673-48_1673-44del ENSP00000328531.4:n.1673-48_1673-44del
ENST00000262186.9:c.2693-48_2693-44del ENSP00000262186.5:n.2693-48_2693-44del
ENST00000330883.8:c.1673-48_1673-44del ENSP00000328531.4:n.1673-48_1673-44del
NM_000238.3:c.2693-48_2693-44del , LRG_288t1:c.2693-48_2693-44del NP_000229.1:n.2693-48_2693-44del
NM_172057.2:c.1673-48_1673-44del , LRG_288t3:c.1673-48_1673-44del NP_742054.1:n.1673-48_1673-44del
XM_011516185.1:c.2393-48_2393-44del XP_011514487.1:n.2393-48_2393-44del
XM_011516186.1:c.2693-235_2693-231del XP_011514488.1:n.2693-235_2693-231del
XM_011516185.2:c.2393-48_2393-44del XP_011514487.1:n.2393-48_2393-44del
XM_011516186.3:c.2693-235_2693-231del XP_011514488.1:n.2693-235_2693-231del
XM_017012195.1:c.2543-48_2543-44del XP_016867684.1:n.2543-48_2543-44del
XM_017012196.1:c.2516-48_2516-44del XP_016867685.1:n.2516-48_2516-44del
NM_000238.4:c.2693-48_2693-44del MANE Select NP_000229.1:n.2693-48_2693-44del
NM_172057.3:c.1673-48_1673-44del NP_742054.1:n.1673-48_1673-44del