HGVS | Genome Assembly |
---|---|
NC_000008.11:g.23682828del , CM000670.2:g.23682828del | GRCh38 |
NC_000008.10:g.23540341del , CM000670.1:g.23540341del | GRCh37 |
NC_000008.9:g.23596286del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380871.5:c.65del MANE Select | ENSP00000370253.4:p.Pro22ArgfsTer? | |
ENST00000380871.4:c.65del | ENSP00000370253.4:p.Pro22ArgfsTer? | |
ENST00000523261.1:c.33+32del | ENSP00000429729.1:n.33+32del | |
NM_001256339.1:c.33+32del | NP_001243268.1:n.33+32del | |
NM_006167.3:c.65del | NP_006158.2:p.Pro22ArgfsTer? | |
NR_046072.1:n.18+79del | ||
XR_001745842.1:n.1312+14078del | ||
NM_006167.4:c.65del MANE Select | NP_006158.2:p.Pro22ArgfsTer? | |
NR_046072.2:n.35+79del |