HGVS | Genome Assembly |
---|---|
NC_000006.12:g.10874247_10874248insGG , CM000668.2:g.10874247_10874248insGG | GRCh38 |
NC_000006.11:g.10874480_10874481insGG , CM000668.1:g.10874480_10874481insGG | GRCh37 |
NC_000006.10:g.10982466_10982467insGG | NCBI36 |
NG_008970.1:g.12618_12619insCC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000379491.5:c.1268_1269insCC MANE Select | ENSP00000368805.4:p.Met423IlefsTer13 | |
ENST00000379491.4:c.1268_1269insCC | ENSP00000368805.4:p.Met423IlefsTer13 | |
ENST00000480294.1:c.101-17266_101-17265insGG | ENSP00000417929.1:n.101-17266_101-17265in... | |
NM_004752.3:c.1268_1269insCC | NP_004743.1:p.Met423IlefsTer13 | |
XM_011514991.1:c.1268_1269insCC | XP_011513293.1:p.Met423IlefsTer13 | |
NM_004752.4:c.1268_1269insCC MANE Select | NP_004743.1:p.Met423IlefsTer13 |