HGVS | Genome Assembly |
---|---|
NC_000006.12:g.160553486_160553489delinsTGTC , CM000668.2:g.160553486_160553489delinsTGTC | GRCh38 |
NC_000006.11:g.160974518_160974521delinsTGTC , CM000668.1:g.160974518_160974521delinsTGTC | GRCh37 |
NC_000006.10:g.160894508_160894511delinsTGTC | NCBI36 |
NG_016147.1:g.117887_117890delinsGACA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000316300.10:c.4973+2536_4973+2539delinsGACA MANE Select | ENSP00000321334.6:n.4973+2536_4973+2539delinsGACA | |
ENST00000316300.9:c.4973+2536_4973+2539delinsGACA | ENSP00000321334.5:n.4973+2536_4973+2539delinsGACA | |
NM_005577.2:c.4973+2536_4973+2539delinsGACA | NP_005568.2:n.4973+2536_4973+2539delinsGACA | |
NM_005577.3:c.4973+2536_4973+2539delinsGACA | NP_005568.2:n.4973+2536_4973+2539delinsGACA | |
NM_005577.4:c.4973+2536_4973+2539delinsGACA MANE Select | NP_005568.2:n.4973+2536_4973+2539delinsGACA |