Canonical Allele Identifier: CA2695208799
Gene: KCNH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150947597_150947606del , CM000669.2:g.150947597_150947606del GRCh38
NC_000007.13:g.150644685_150644694del , CM000669.1:g.150644685_150644694del GRCh37
NC_000007.12:g.150275618_150275627del NCBI36
NG_008916.1:g.35322_35331del , LRG_288:g.35322_35331del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684241.1:n.3798+1_3798+10del
ENST00000262186.10:c.2965+1_2965+10del
ENST00000330883.9:c.1945+1_1945+10del
ENST00000262186.9:c.2965+1_2965+10del
ENST00000330883.8:c.1945+1_1945+10del
NM_000238.3:c.2965+1_2965+10del , LRG_288t1:c.2965+1_2965+10del
NM_172057.2:c.1945+1_1945+10del , LRG_288t3:c.1945+1_1945+10del
XM_011516185.1:c.2665+1_2665+10del
XM_011516186.1:c.*45+1_*45+10del
XM_011516185.2:c.2665+1_2665+10del
XM_011516186.3:c.*45+1_*45+10del
XM_017012195.1:c.2815+1_2815+10del
XM_017012196.1:c.2788+1_2788+10del
NM_000238.4:c.2965+1_2965+10del
NM_172057.3:c.1945+1_1945+10del