HGVS | Genome Assembly |
---|---|
NC_000014.9:g.28767600_28767602del , CM000676.2:g.28767600_28767602del | GRCh38 |
NC_000014.8:g.29236806_29236808del , CM000676.1:g.29236806_29236808del | GRCh37 |
NC_000014.7:g.28306557_28306559del | NCBI36 |
NG_009367.1:g.5520_5522del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706482.1:c.321_323del | ENSP00000516406.1:p.Pro108del | |
ENST00000313071.7:c.321_323del MANE Select | ENSP00000339004.3:p.Pro108del | |
ENST00000313071.6:c.321_323del | ENSP00000339004.3:p.Pro108del | |
NM_005249.4:c.321_323del | NP_005240.3:p.Pro108del | |
NM_005249.5:c.321_323del MANE Select | NP_005240.3:p.Pro108del |