HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131890514_131890515delinsTG , CM000668.2:g.131890514_131890515delinsTG | GRCh38 |
NC_000006.11:g.132211654_132211655delinsTG , CM000668.1:g.132211654_132211655delinsTG | GRCh37 |
NC_000006.10:g.132253347_132253348delinsTG | NCBI36 |
NG_008206.1:g.87499_87500delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684674.1:n.1212_1213delinsTG | ||
ENST00000647893.1:c.*3_*4delinsTG MANE Select | ENSP00000498074.1:n.*3_*4delinsTG | |
ENST00000360971.6:c.*3_*4delinsTG | ENSP00000354238.2:n.*3_*4delinsTG | |
ENST00000513998.5:c.*1618_*1619delinsTG | ENSP00000422424.1:n.*1618_*1619delinsTG | |
NM_006208.2:c.*3_*4delinsTG | NP_006199.2:n.*3_*4delinsTG | |
XM_011535896.1:c.*3_*4delinsTG | XP_011534198.1:n.*3_*4delinsTG | |
NM_006208.3:c.*3_*4delinsTG MANE Select | NP_006199.2:n.*3_*4delinsTG |