HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44389385del , CM000679.2:g.44389385del | GRCh38 |
NC_000017.10:g.42466753del , CM000679.1:g.42466753del | GRCh37 |
NC_000017.9:g.39822279del | NCBI36 |
NG_008331.1:g.5123del , LRG_479:g.5123del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262407.6:c.91del MANE Select | ENSP00000262407.5:p.Ala31ProfsTer2 | |
ENST00000262407.5:c.91del | ENSP00000262407.5:p.Ala31ProfsTer2 | |
NM_000419.3:c.91del , LRG_479t1:c.91del | NP_000410.2:p.Ala31ProfsTer2 | |
XM_011524749.1:c.91del | XP_011523051.1:p.Ala31ProfsTer2 | |
XM_011524750.1:c.91del | XP_011523052.1:p.Ala31ProfsTer2 | |
NM_000419.4:c.91del | NP_000410.2:p.Ala31ProfsTer2 | |
NM_000419.5:c.91del MANE Select | NP_000410.2:p.Ala31ProfsTer2 |