HGVS | Genome Assembly |
---|---|
NC_000008.11:g.37966201_37966205del , CM000670.2:g.37966201_37966205del | GRCh38 |
NC_000008.10:g.37823719_37823723del , CM000670.1:g.37823719_37823723del | GRCh37 |
NC_000008.9:g.37942876_37942880del | NCBI36 |
NG_011936.1:g.5462_5466del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000345060.5:c.265_269del MANE Select | ENSP00000343782.3:p.Leu89GlyfsTer? | |
ENST00000520341.2:n.393_397del | ||
ENST00000345060.4:c.265_269del | ENSP00000343782.3:p.Leu89GlyfsTer? | |
ENST00000614635.1:c.265_269del | ENSP00000480325.1:p.Leu89GlyfsTer? | |
NM_000025.2:c.265_269del | NP_000016.1:p.Leu89GlyfsTer? | |
NM_000025.3:c.265_269del MANE Select | NP_000016.1:p.Leu89GlyfsTer? |