HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131890616_131890626del , CM000668.2:g.131890616_131890626del | GRCh38 |
NC_000006.11:g.132211756_132211766del , CM000668.1:g.132211756_132211766del | GRCh37 |
NC_000006.10:g.132253449_132253459del | NCBI36 |
NG_008206.1:g.87601_87611del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684674.1:n.1314_1324del | ||
ENST00000647893.1:c.*105_*115del MANE Select | ENSP00000498074.1:n.*105_*115del | |
ENST00000360971.6:c.*105_*115del | ENSP00000354238.2:n.*105_*115del | |
ENST00000513998.5:c.*1720_*1730del | ENSP00000422424.1:n.*1720_*1730del | |
NM_006208.2:c.*105_*115del | NP_006199.2:n.*105_*115del | |
XM_011535896.1:c.*105_*115del | XP_011534198.1:n.*105_*115del | |
NM_006208.3:c.*105_*115del MANE Select | NP_006199.2:n.*105_*115del |