HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038084_52038085delinsCG , CM000666.2:g.52038084_52038085delinsCG | GRCh38 |
NC_000004.11:g.52904250_52904251delinsCG , CM000666.1:g.52904250_52904251delinsCG | GRCh37 |
NC_000004.10:g.52599007_52599008delinsCG | NCBI36 |
NG_008891.1:g.5235_5236delinsCG , LRG_204:g.5235_5236delinsCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.33+142_33+143delinsCG MANE Select | ENSP00000370839.6:n.33+142_33+143delinsCG | |
ENST00000381431.9:c.33+142_33+143delinsCG | ENSP00000370839.5:n.33+142_33+143delinsCG | |
ENST00000506357.5:c.19+142_19+143delinsCG | ||
NM_000232.4:c.33+142_33+143delinsCG , LRG_204t1:c.33+142_33+143delinsCG | NP_000223.1:n.33+142_33+143delinsCG | |
XM_011534403.1:c.33+142_33+143delinsCG | XP_011532705.1:n.33+142_33+143delinsCG | |
NM_000232.5:c.33+142_33+143delinsCG MANE Select | NP_000223.1:n.33+142_33+143delinsCG |