HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571692_154571693insT , CM000663.2:g.154571692_154571693insT | GRCh38 |
NC_000001.10:g.154544168_154544169insT , CM000663.1:g.154544168_154544169insT | GRCh37 |
NC_000001.9:g.152810792_152810793insT | NCBI36 |
NG_008027.1:g.8912_8913insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.869_870insT MANE Select | ENSP00000357461.3:p.Ser291LeufsTer? | |
ENST00000636034.1:c.869_870insT | ENSP00000489703.1:p.Ser291LeufsTer? | |
ENST00000637900.1:c.875_876insT | ENSP00000490474.1:p.Ser293LeufsTer? | |
ENST00000368476.3:c.869_870insT | ENSP00000357461.3:p.Ser291LeufsTer? | |
NM_000748.2:c.869_870insT | NP_000739.1:p.Ser291LeufsTer? | |
XM_017000180.2:c.359_360insT | XP_016855669.1:p.Ser121LeufsTer? | |
XR_001736952.2:n.1121_1122insT | ||
NM_000748.3:c.869_870insT MANE Select | NP_000739.1:p.Ser291LeufsTer? |