HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038184_52038185delinsTC , CM000666.2:g.52038184_52038185delinsTC | GRCh38 |
NC_000004.11:g.52904350_52904351delinsTC , CM000666.1:g.52904350_52904351delinsTC | GRCh37 |
NC_000004.10:g.52599107_52599108delinsTC | NCBI36 |
NG_008891.1:g.5135_5136delinsGA , LRG_204:g.5135_5136delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.33+42_33+43delinsGA MANE Select | ENSP00000370839.6:n.33+42_33+43delinsGA | |
ENST00000381431.9:c.33+42_33+43delinsGA | ENSP00000370839.5:n.33+42_33+43delinsGA | |
ENST00000506357.5:c.19+42_19+43delinsGA | ||
NM_000232.4:c.33+42_33+43delinsGA , LRG_204t1:c.33+42_33+43delinsGA | NP_000223.1:n.33+42_33+43delinsGA | |
XM_011534403.1:c.33+42_33+43delinsGA | XP_011532705.1:n.33+42_33+43delinsGA | |
NM_000232.5:c.33+42_33+43delinsGA MANE Select | NP_000223.1:n.33+42_33+43delinsGA |