HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29073074_29073075insAAT , CM000664.2:g.29073074_29073075insAAT | GRCh38 |
NC_000002.11:g.29295940_29295941insAAT , CM000664.1:g.29295940_29295941insAAT | GRCh37 |
NC_000002.10:g.29149444_29149445insAAT | NCBI36 |
NG_021427.1:g.6187_6188insATT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.1187_1188insATT MANE Select | ENSP00000332809.4:p.Thr396_Trp397insPhe | |
ENST00000331664.5:c.1187_1188insATT | ENSP00000332809.4:p.Thr396_Trp397insPhe | |
NM_001029883.2:c.1187_1188insATT | NP_001025054.1:p.Thr396_Trp397insPhe | |
XM_011532826.1:c.1187_1188insATT | XP_011531128.1:p.Thr396_Trp397insPhe | |
XR_939901.1:n.185+3907_185+3908insAAT | ||
XR_939902.1:n.173+3919_173+3920insAAT | ||
NM_001029883.3:c.1187_1188insATT MANE Select | NP_001025054.1:p.Thr396_Trp397insPhe |