HGVS | Genome Assembly |
---|---|
NC_000016.10:g.17138305del , CM000678.2:g.17138305del | GRCh38 |
NC_000016.9:g.17232162del , CM000678.1:g.17232162del | GRCh37 |
NC_000016.8:g.17139663del | NCBI36 |
NG_015843.1:g.337579del | |
NG_015843.2:g.337579del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261381.7:c.1764+52del MANE Select | ENSP00000261381.6:n.1764+52del | |
ENST00000261381.6:c.1764+52del | ENSP00000261381.6:n.1764+52del | |
NM_022166.3:c.1764+52del | NP_071449.1:n.1764+52del | |
XM_011522574.1:c.1764+52del | XP_011520876.1:n.1764+52del | |
XR_933140.1:n.399del | ||
XR_933141.1:n.238del | ||
XR_933143.1:n.300del | ||
NR_135179.1:n.210del | ||
XM_017023539.2:c.1764+52del | XP_016879028.1:n.1764+52del | |
XM_017023540.2:c.1764+52del | XP_016879029.1:n.1764+52del | |
NM_022166.4:c.1764+52del MANE Select | NP_071449.1:n.1764+52del |