HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35848061del , CM000681.2:g.35848061del | GRCh38 |
NC_000019.9:g.36338963del , CM000681.1:g.36338963del | GRCh37 |
NC_000019.8:g.41030803del | NCBI36 |
NG_013356.2:g.26229del , LRG_693:g.26229del | |
NG_051206.1:g.1427del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378910.10:c.1422del MANE Select | ENSP00000368190.4:p.Ser475ProfsTer11 | |
ENST00000353632.6:c.1422del | ENSP00000343634.5:p.Ser475ProfsTer11 | |
ENST00000378910.9:c.1422del | ENSP00000368190.4:p.Ser475ProfsTer11 | |
ENST00000592132.1:n.429del | ||
NM_004646.3:c.1422del , LRG_693t1:c.1422del | NP_004637.1:p.Ser475ProfsTer11 | |
NM_004646.4:c.1422del MANE Select | NP_004637.1:p.Ser475ProfsTer11 |