HGVS | Genome Assembly |
---|---|
NC_000017.11:g.39665858_39665881del , CM000679.2:g.39665858_39665881del | GRCh38 |
NC_000017.10:g.37822111_37822134del , CM000679.1:g.37822111_37822134del | GRCh37 |
NC_000017.9:g.35075637_35075660del | NCBI36 |
NG_008892.1:g.5513_5536del , LRG_210:g.5513_5536del | |
NG_042278.1:g.2878_2901del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000309889.3:c.253_276del MANE Select | ENSP00000312624.2:p.Tyr85_Pro92del | |
ENST00000309889.2:c.253_276del | ENSP00000312624.2:p.Tyr85_Pro92del | |
ENST00000578283.1:c.181_204del | ||
NM_003673.3:c.253_276del , LRG_210t1:c.253_276del | NP_003664.1:p.Tyr85_Pro92del | |
NM_003673.4:c.253_276del MANE Select | NP_003664.1:p.Tyr85_Pro92del |