HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218882283del , CM000664.2:g.218882283del | GRCh38 |
NC_000002.11:g.219747005del , CM000664.1:g.219747005del | GRCh37 |
NC_000002.10:g.219455249del | NCBI36 |
NG_012179.1:g.6751del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258411.8:c.236del MANE Select | ENSP00000258411.3:p.Pro79LeufsTer? | |
ENST00000258411.7:c.236del | ENSP00000258411.3:p.Pro79LeufsTer? | |
ENST00000458582.1:c.123del | ||
NM_025216.2:c.236del | NP_079492.2:p.Pro79LeufsTer? | |
XM_011511928.1:c.185del | XP_011510230.1:p.Pro62LeufsTer? | |
XM_011511929.1:c.140del | XP_011510231.1:p.Pro47LeufsTer? | |
XM_011511930.1:c.236del | XP_011510232.1:p.Pro79LeufsTer? | |
XM_011511929.2:c.140del | XP_011510231.1:p.Pro47LeufsTer? | |
NM_025216.3:c.236del MANE Select | NP_079492.2:p.Pro79LeufsTer? |