HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21176597_21176598insA , CM000674.2:g.21176597_21176598insA | GRCh38 |
NC_000012.11:g.21329531_21329532insA , CM000674.1:g.21329531_21329532insA | GRCh37 |
NC_000012.10:g.21220798_21220799insA | NCBI36 |
NG_011745.1:g.50404_50405insA , LRG_1022:g.50404_50405insA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.360-179_360-178insA MANE Select | ENSP00000256958.2:n.360-179_360-178insA | |
ENST00000256958.2:c.360-179_360-178insA | ENSP00000256958.2:n.360-179_360-178insA | |
ENST00000543498.5:c.426-179_426-178insA | ||
NM_006446.4:c.360-179_360-178insA , LRG_1022t1:c.360-179_360-178insA | NP_006437.3:n.360-179_360-178insA | |
NM_006446.5:c.360-179_360-178insA MANE Select | NP_006437.3:n.360-179_360-178insA |