HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154953953del , CM000685.2:g.154953953del | GRCh38 |
NC_000023.10:g.154182228del , CM000685.1:g.154182228del | GRCh37 |
NC_000023.9:g.153835422del | NCBI36 |
NG_011403.1:g.73774del | |
NG_011403.2:g.73774del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.1845del MANE Select | ENSP00000353393.4:p.Asn616IlefsTer? | |
ENST00000647125.1:c.*1721del | ENSP00000496062.1:n.*1721del | |
ENST00000360256.8:c.1845del | ENSP00000353393.4:p.Asn616IlefsTer? | |
NM_000132.3:c.1845del | NP_000123.1:p.Asn616IlefsTer? | |
XM_011531126.1:c.1740del | XP_011529428.1:p.Asn581IlefsTer? | |
NM_000132.4:c.1845del MANE Select | NP_000123.1:p.Asn616IlefsTer? |