HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107710146_107710147insG , CM000669.2:g.107710146_107710147insG | GRCh38 |
NC_000007.13:g.107350591_107350592insG , CM000669.1:g.107350591_107350592insG | GRCh37 |
NC_000007.12:g.107137827_107137828insG | NCBI36 |
NG_008489.1:g.54512_54513insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644269.2:c.2182_2183insG MANE Select | ENSP00000494017.1:p.Tyr728Ter | |
ENST00000644846.1:c.838_839insG | ||
ENST00000265715.7:c.2182_2183insG | ENSP00000265715.3:p.Tyr728Ter | |
ENST00000492030.2:n.377-9_377-8insG | ||
NM_000441.1:c.2182_2183insG | NP_000432.1:p.Tyr728Ter | |
XM_005250425.1:c.2182_2183insG | XP_005250482.1:p.Tyr728Ter | |
XM_005250425.2:c.2182_2183insG | XP_005250482.1:p.Tyr728Ter | |
XM_017012318.1:c.2104_2105insG | XP_016867807.1:p.Tyr702Ter | |
NM_000441.2:c.2182_2183insG MANE Select | NP_000432.1:p.Tyr728Ter |