HGVS | Genome Assembly |
---|---|
NC_000020.11:g.31819979_31819989del , CM000682.2:g.31819979_31819989del | GRCh38 |
NC_000020.10:g.30407782_30407792del , CM000682.1:g.30407782_30407792del | GRCh37 |
NC_000020.9:g.29871443_29871453del | NCBI36 |
NG_012847.1:g.5605_5615del , LRG_392:g.5605_5615del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375985.5:c.53-147_53-137del MANE Select | ENSP00000365152.4:n.53-147_53-137del | |
ENST00000375985.4:c.53-147_53-137del | ENSP00000365152.4:n.53-147_53-137del | |
ENST00000375994.6:c.53-147_53-137del | ENSP00000365162.2:n.53-147_53-137del | |
NM_033118.3:c.53-147_53-137del , LRG_392t1:c.53-147_53-137del | NP_149109.1:n.53-147_53-137del | |
XR_244155.1:n.218-147_218-137del | ||
NM_033118.4:c.53-147_53-137del MANE Select | NP_149109.1:n.53-147_53-137del |