HGVS | Genome Assembly |
---|---|
NC_000008.11:g.37965839del , CM000670.2:g.37965839del | GRCh38 |
NC_000008.10:g.37823357del , CM000670.1:g.37823357del | GRCh37 |
NC_000008.9:g.37942514del | NCBI36 |
NG_011936.1:g.5828del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000345060.5:c.631del MANE Select | ENSP00000343782.3:p.Val211SerfsTer9 | |
ENST00000520341.2:n.759del | ||
ENST00000647937.1:c.115del | ENSP00000497740.1:p.Val39SerfsTer9 | |
ENST00000345060.4:c.631del | ENSP00000343782.3:p.Val211SerfsTer9 | |
ENST00000614635.1:c.631del | ENSP00000480325.1:p.Val211SerfsTer9 | |
NM_000025.2:c.631del | NP_000016.1:p.Val211SerfsTer9 | |
NM_000025.3:c.631del MANE Select | NP_000016.1:p.Val211SerfsTer9 |