HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48364923del , CM000675.2:g.48364923del | GRCh38 |
NC_000013.10:g.48939059del , CM000675.1:g.48939059del | GRCh37 |
NC_000013.9:g.47837060del | NCBI36 |
NG_009009.1:g.66177del , LRG_517:g.66177del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.891del MANE Select | ENSP00000267163.4:p.Pro298LeufsTer3 | |
ENST00000650461.1:c.891del | ENSP00000497193.1:p.Pro298LeufsTer3 | |
ENST00000267163.4:c.891del | ENSP00000267163.4:p.Pro298LeufsTer3 | |
NM_000321.2:c.891del , LRG_517t1:c.891del | NP_000312.2:p.Pro298LeufsTer3 | |
XM_011535171.1:c.630del | XP_011533473.1:p.Pro211LeufsTer3 | |
XM_011535171.2:c.630del | XP_011533473.1:p.Pro211LeufsTer3 | |
XR_002957522.1:n.175del | ||
NM_000321.3:c.891del MANE Select | NP_000312.2:p.Pro298LeufsTer3 |