HGVS | Genome Assembly |
---|---|
NC_000001.11:g.183207983_183207984delinsAT , CM000663.2:g.183207983_183207984delinsAT | GRCh38 |
NC_000001.10:g.183177118_183177119delinsAT , CM000663.1:g.183177118_183177119delinsAT | GRCh37 |
NC_000001.9:g.181443741_181443742delinsAT | NCBI36 |
NG_007079.2:g.26720_26721delinsAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264144.5:c.182_183delinsAT MANE Select | ENSP00000264144.4:p.Asp61= | |
ENST00000264144.4:c.182_183delinsAT | ENSP00000264144.4:p.Asp61= | |
ENST00000493293.5:c.182_183delinsAT | ENSP00000432063.1:p.Asp61= | |
NM_005562.2:c.182_183delinsAT | NP_005553.2:p.Asp61= | |
NM_018891.2:c.182_183delinsAT | NP_061486.2:p.Asp61= | |
XM_017001273.2:c.182_183delinsAT | XP_016856762.1:p.Asp61= | |
NM_005562.3:c.182_183delinsAT MANE Select | NP_005553.2:p.Asp61= | |
NM_018891.3:c.182_183delinsAT | NP_061486.2:p.Asp61= |