HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571698_154571700delinsTCG , CM000663.2:g.154571698_154571700delinsTCG | GRCh38 |
NC_000001.10:g.154544174_154544176delinsTCG , CM000663.1:g.154544174_154544176delinsTCG | GRCh37 |
NC_000001.9:g.152810798_152810800delinsTCG | NCBI36 |
NG_008027.1:g.8918_8920delinsTCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.875_877delinsTCG MANE Select | ENSP00000357461.3:p.Leu292= | |
ENST00000636034.1:c.875_877delinsTCG | ENSP00000489703.1:p.Leu292= | |
ENST00000637900.1:c.881_883delinsTCG | ENSP00000490474.1:p.Leu294= | |
ENST00000368476.3:c.875_877delinsTCG | ENSP00000357461.3:p.Leu292= | |
NM_000748.2:c.875_877delinsTCG | NP_000739.1:p.Leu292= | |
XM_017000180.2:c.365_367delinsTCG | XP_016855669.1:p.Leu122= | |
XR_001736952.2:n.1127_1129delinsTCG | ||
NM_000748.3:c.875_877delinsTCG MANE Select | NP_000739.1:p.Leu292= |