HGVS | Genome Assembly |
---|---|
NC_000002.12:g.27085166del , CM000664.2:g.27085166del | GRCh38 |
NC_000002.11:g.27308034del , CM000664.1:g.27308034del | GRCh37 |
NC_000002.10:g.27161538del | NCBI36 |
NG_012199.1:g.3424del | |
NG_046849.1:g.11600del | |
NG_012199.2:g.3424del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380320.9:c.2582del MANE Select | ENSP00000369677.4:p.Glu861GlyfsTer17 | |
ENST00000380320.8:c.2582del | ENSP00000369677.4:p.Glu861GlyfsTer17 | |
ENST00000433140.1:c.574del | ||
NM_007046.3:c.2582del | NP_008977.1:p.Glu861GlyfsTer17 | |
XM_006711928.2:c.2575+158del | XP_006711991.1:n.2575+158del | |
NM_007046.4:c.2582del MANE Select | NP_008977.1:p.Glu861GlyfsTer17 |