HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119672444del , CM000672.2:g.119672444del | GRCh38 |
NC_000010.10:g.121431956del , CM000672.1:g.121431956del | GRCh37 |
NC_000010.9:g.121421946del | NCBI36 |
NG_016125.1:g.26075del , LRG_742:g.26075del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369085.8:c.697del MANE Select | ENSP00000358081.4:p.Tyr233ThrfsTer? | |
ENST00000369085.7:c.697del | ENSP00000358081.3:p.Tyr233ThrfsTer? | |
ENST00000450186.1:c.523del | ENSP00000410036.1:p.Tyr175ThrfsTer? | |
NM_004281.3:c.697del , LRG_742t1:c.697del | NP_004272.2:p.Tyr233ThrfsTer? | |
XM_005270287.1:c.697del | XP_005270344.1:p.Tyr233ThrfsTer? | |
XM_005270287.2:c.697del | XP_005270344.1:p.Tyr233ThrfsTer? | |
NM_004281.4:c.697del MANE Select | NP_004272.2:p.Tyr233ThrfsTer? |