HGVS | Genome Assembly |
---|---|
NC_000012.12:g.120739715_120739716insACCA , CM000674.2:g.120739715_120739716insACCA | GRCh38 |
NC_000012.11:g.121177518_121177519insACCA , CM000674.1:g.121177518_121177519insACCA | GRCh37 |
NC_000012.10:g.119661901_119661902insACCA | NCBI36 |
NG_007991.1:g.18948_18949insACCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242592.9:c.*267_*268insACCA MANE Select | ENSP00000242592.4:n.*267_*268insACCA | |
ENST00000242592.8:c.*267_*268insACCA | ENSP00000242592.4:n.*267_*268insACCA | |
NM_000017.3:c.*267_*268insACCA | NP_000008.1:n.*267_*268insACCA | |
NM_001302554.1:c.*267_*268insACCA | NP_001289483.1:n.*267_*268insACCA | |
NM_000017.4:c.*267_*268insACCA MANE Select | NP_000008.1:n.*267_*268insACCA | |
NM_001302554.2:c.*267_*268insACCA | NP_001289483.1:n.*267_*268insACCA |