HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461685_122461686insTCC , CM000672.2:g.122461685_122461686insTCC | GRCh38 |
NC_000010.10:g.124221201_124221202insTCC , CM000672.1:g.124221201_124221202insTCC | GRCh37 |
NC_000010.9:g.124211191_124211192insTCC | NCBI36 |
NG_011554.1:g.5161_5162insTCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.33_34insTCC MANE Select | ENSP00000357980.3:p.Leu11_Leu12insSer | |
ENST00000648167.1:c.154+2976_154+2977insTCC | ENSP00000498033.1:n.154+2976_154+2977insTCC | |
ENST00000368984.7:c.33_34insTCC | ENSP00000357980.3:p.Leu11_Leu12insSer | |
NM_002775.4:c.33_34insTCC | NP_002766.1:p.Leu11_Leu12insSer | |
NM_002775.5:c.33_34insTCC MANE Select | NP_002766.1:p.Leu11_Leu12insSer |