HGVS | Genome Assembly |
---|---|
NC_000010.11:g.1410636_1410643delinsCATCTGCT , CM000672.2:g.1410636_1410643delinsCATCTGCT | GRCh38 |
NC_000010.10:g.1452831_1452838delinsCATCTGCT , CM000672.1:g.1452831_1452838delinsCATCTGCT | GRCh37 |
NC_000010.9:g.1442831_1442838delinsCATCTGCT | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000381312.6:c.101-31483_101-31476delinsAGCAGATG MANE Select | ENSP00000370713.1:n.101-31483_101-31476de... | |
ENST00000381312.5:c.101-31483_101-31476delinsAGCAGATG | ENSP00000370713.1:n.101-31483_101-31476de... | |
NM_018702.3:c.101-31483_101-31476delinsAGCAGATG | NP_061172.1:n.101-31483_101-31476delinsAG... | |
XR_930468.1:n.449-31483_449-31476delinsAGCAGATG | ||
NM_018702.4:c.101-31483_101-31476delinsAGCAGATG MANE Select | NP_061172.1:n.101-31483_101-31476delinsAG... |