HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663181_36663188del , CM000676.2:g.36663181_36663188del | GRCh38 |
NC_000014.8:g.37132386_37132393del , CM000676.1:g.37132386_37132393del | GRCh37 |
NC_000014.7:g.36202137_36202144del | NCBI36 |
NG_013357.1:g.10614_10621del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361487.7:c.289_296del MANE Select | ENSP00000355245.6:p.Ile97LeufsTer? | |
ENST00000361487.6:c.289_296del | ENSP00000355245.6:p.Ile97LeufsTer? | |
ENST00000402703.6:c.289_296del | ENSP00000384817.2:p.Ile97LeufsTer? | |
ENST00000554201.1:c.-273_-266del | ENSP00000450434.1:n.-273_-266del | |
NM_006194.3:c.289_296del | NP_006185.1:p.Ile97LeufsTer? | |
NM_001372076.1:c.289_296del MANE Select | NP_001359005.1:p.Ile97LeufsTer? | |
NM_006194.4:c.289_296del | NP_006185.1:p.Ile97LeufsTer? |