HGVS | Genome Assembly |
---|---|
NC_000002.12:g.169487810_169487811delinsCG , CM000664.2:g.169487810_169487811delinsCG | GRCh38 |
NC_000002.11:g.170344320_170344321delinsCG , CM000664.1:g.170344320_170344321delinsCG | GRCh37 |
NC_000002.10:g.170052566_170052567delinsCG | NCBI36 |
NG_011567.1:g.13315_13316delinsCG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000295240.8:c.213_214delinsCG MANE Select | ENSP00000295240.3:p.Val71= | |
ENST00000295240.7:c.213_214delinsCG | ENSP00000295240.3:p.Val71= | |
ENST00000392663.6:c.213_214delinsCG | ENSP00000376431.2:p.Val71= | |
ENST00000443151.1:c.143-177_143-176delinsCG | ENSP00000406182.1:n.143-177_143-176delins... | |
ENST00000475571.1:n.49_50delinsCG | ||
ENST00000513963.1:c.213_214delinsCG | ENSP00000424363.1:p.Val71= | |
NM_152384.2:c.213_214delinsCG | NP_689597.1:p.Val71= | |
NM_152384.3:c.213_214delinsCG MANE Select | NP_689597.1:p.Val71= |