HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91055996_91055997insAAATAA , CM000674.2:g.91055996_91055997insAAATAA | GRCh38 |
NC_000012.11:g.91449773_91449774insAAATAA , CM000674.1:g.91449773_91449774insAAATAA | GRCh37 |
NC_000012.10:g.89973904_89973905insAAATAA | NCBI36 |
NG_021223.1:g.7358_7359insTTATTT , LRG_538:g.7358_7359insTTATTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266719.4:c.285_286insTTATTT MANE Select | ENSP00000266719.3:p.Thr95_Gln96insLeuPhe | |
ENST00000266719.3:c.285_286insTTATTT | ENSP00000266719.3:p.Thr95_Gln96insLeuPhe | |
NM_007035.3:c.285_286insTTATTT , LRG_538t1:c.285_286insTTATTT | NP_008966.1:p.Thr95_Gln96insLeuPhe | |
XM_011537781.1:c.285_286insTTATTT | XP_011536083.1:p.Thr95_Gln96insLeuPhe | |
NM_007035.4:c.285_286insTTATTT MANE Select | NP_008966.1:p.Thr95_Gln96insLeuPhe |