HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584097_41584099delinsTTG , CM000679.2:g.41584097_41584099delinsTTG | GRCh38 |
NC_000017.10:g.39740349_39740351delinsTTG , CM000679.1:g.39740349_39740351delinsTTG | GRCh37 |
NC_000017.9:g.36993875_36993877delinsTTG | NCBI36 |
NG_008624.1:g.7797_7799delinsCAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.765+158_765+160delinsCAA MANE Select | ENSP00000167586.6:n.765+158_765+160delinsCAA | |
ENST00000167586.6:c.765+158_765+160delinsCAA | ENSP00000167586.6:n.765+158_765+160delinsCAA | |
ENST00000476662.1:n.215+158_215+160delinsCAA | ||
NM_000526.4:c.765+158_765+160delinsCAA | NP_000517.2:n.765+158_765+160delinsCAA | |
NM_000526.5:c.765+158_765+160delinsCAA MANE Select | NP_000517.3:n.765+158_765+160delinsCAA |