HGVS | Genome Assembly |
---|---|
NC_000003.12:g.87259660_87259661insAAA , CM000665.2:g.87259660_87259661insAAA | GRCh38 |
NC_000003.11:g.87308810_87308811insAAA , CM000665.1:g.87308810_87308811insAAA | GRCh37 |
NC_000003.10:g.87391500_87391501insAAA | NCBI36 |
NG_008225.2:g.21929_21930insTTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344265.8:c.*235_*236insTTT | ENSP00000342931.3:n.*235_*236insTTT | |
ENST00000350375.7:c.*235_*236insTTT MANE Select | ENSP00000263781.2:n.*235_*236insTTT | |
ENST00000350375.6:c.*235_*236insTTT | ENSP00000263781.2:n.*235_*236insTTT | |
NM_000306.3:c.*235_*236insTTT | NP_000297.1:n.*235_*236insTTT | |
NM_001122757.2:c.*235_*236insTTT | NP_001116229.1:n.*235_*236insTTT | |
NM_000306.4:c.*235_*236insTTT MANE Select | NP_000297.1:n.*235_*236insTTT | |
NM_001122757.3:c.*235_*236insTTT | NP_001116229.1:n.*235_*236insTTT |