HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571698_154571701delinsTCGA , CM000663.2:g.154571698_154571701delinsTCGA | GRCh38 |
NC_000001.10:g.154544174_154544177delinsTCGA , CM000663.1:g.154544174_154544177delinsTCGA | GRCh37 |
NC_000001.9:g.152810798_152810801delinsTCGA | NCBI36 |
NG_008027.1:g.8918_8921delinsTCGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.875_878delinsTCGA MANE Select | ENSP00000357461.3:p.Leu292= | |
ENST00000636034.1:c.875_878delinsTCGA | ENSP00000489703.1:p.Leu292= | |
ENST00000637900.1:c.881_884delinsTCGA | ENSP00000490474.1:p.Leu294= | |
ENST00000368476.3:c.875_878delinsTCGA | ENSP00000357461.3:p.Leu292= | |
NM_000748.2:c.875_878delinsTCGA | NP_000739.1:p.Leu292= | |
XM_017000180.2:c.365_368delinsTCGA | XP_016855669.1:p.Leu122= | |
XR_001736952.2:n.1127_1130delinsTCGA | ||
NM_000748.3:c.875_878delinsTCGA MANE Select | NP_000739.1:p.Leu292= |