HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038091_52038092insA , CM000666.2:g.52038091_52038092insA | GRCh38 |
NC_000004.11:g.52904257_52904258insA , CM000666.1:g.52904257_52904258insA | GRCh37 |
NC_000004.10:g.52599014_52599015insA | NCBI36 |
NG_008891.1:g.5228_5229insT , LRG_204:g.5228_5229insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.33+135_33+136insT MANE Select | ENSP00000370839.6:n.33+135_33+136insT | |
ENST00000381431.9:c.33+135_33+136insT | ENSP00000370839.5:n.33+135_33+136insT | |
ENST00000506357.5:c.19+135_19+136insT | ||
NM_000232.4:c.33+135_33+136insT , LRG_204t1:c.33+135_33+136insT | NP_000223.1:n.33+135_33+136insT | |
XM_011534403.1:c.33+135_33+136insT | XP_011532705.1:n.33+135_33+136insT | |
NM_000232.5:c.33+135_33+136insT MANE Select | NP_000223.1:n.33+135_33+136insT |