HGVS | Genome Assembly |
---|---|
NC_000006.12:g.49459199delinsTT , CM000668.2:g.49459199delinsTT | GRCh38 |
NC_000006.11:g.49426912delinsTT , CM000668.1:g.49426912delinsTT | GRCh37 |
NC_000006.10:g.49534871delinsTT | NCBI36 |
NG_007100.1:g.8941delinsAA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000274813.4:c.268delinsAA MANE Select | ENSP00000274813.3:p.Pro90AsnfsTer14 | |
ENST00000274813.3:c.268delinsAA | ENSP00000274813.3:p.Pro90AsnfsTer14 | |
NM_000255.3:c.268delinsAA | NP_000246.2:p.Pro90AsnfsTer14 | |
XM_005249143.2:c.268delinsAA | XP_005249200.1:p.Pro90AsnfsTer14 | |
XM_005249143.3:c.268delinsAA | XP_005249200.1:p.Pro90AsnfsTer14 | |
NM_000255.4:c.268delinsAA MANE Select | NP_000246.2:p.Pro90AsnfsTer14 |