HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94062814_94062815insA , CM000663.2:g.94062814_94062815insA | GRCh38 |
NC_000001.10:g.94528370_94528371insA , CM000663.1:g.94528370_94528371insA | GRCh37 |
NC_000001.9:g.94300958_94300959insA | NCBI36 |
NG_009073.1:g.63335_63336insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.1761-62_1761-61insT MANE Select | ENSP00000359245.3:n.1761-62_1761-61insT | |
ENST00000649773.1:c.1761-62_1761-61insT | ENSP00000496882.1:n.1761-62_1761-61insT | |
ENST00000370225.3:c.1761-62_1761-61insT | ENSP00000359245.3:n.1761-62_1761-61insT | |
ENST00000536513.5:c.-65+359_-65+360insT | ENSP00000439707.2:n.-65+359_-65+360insT | |
NM_000350.2:c.1761-62_1761-61insT | NP_000341.2:n.1761-62_1761-61insT | |
NM_000350.3:c.1761-62_1761-61insT MANE Select | NP_000341.2:n.1761-62_1761-61insT |