HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24178500_24178501delinsCA , CM000668.2:g.24178500_24178501delinsCA | GRCh38 |
NC_000006.11:g.24178728_24178729delinsCA , CM000668.1:g.24178728_24178729delinsCA | GRCh37 |
NC_000006.10:g.24286707_24286708delinsCA | NCBI36 |
NG_012829.1:g.184552_184553delinsTG | |
NG_012829.2:g.209792_209793delinsTG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378454.8:c.1155_1156delinsTG MANE Select | ENSP00000367715.3:p.Pro385= | |
ENST00000378450.6:c.414_415delinsTG | ENSP00000367711.3:p.Pro138= | |
ENST00000378454.7:c.1155_1156delinsTG | ENSP00000367715.3:p.Pro385= | |
NM_001195610.1:c.1155_1156delinsTG | NP_001182539.1:p.Pro385= | |
NM_016356.4:c.1155_1156delinsTG | NP_057440.2:p.Pro385= | |
NM_016356.5:c.1155_1156delinsTG MANE Select | NP_057440.2:p.Pro385= | |
NM_001195610.2:c.1155_1156delinsTG | NP_001182539.1:p.Pro385= |