HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038094_52038095insCAAA , CM000666.2:g.52038094_52038095insCAAA | GRCh38 |
NC_000004.11:g.52904260_52904261insCAAA , CM000666.1:g.52904260_52904261insCAAA | GRCh37 |
NC_000004.10:g.52599017_52599018insCAAA | NCBI36 |
NG_008891.1:g.5225_5226insTTTG , LRG_204:g.5225_5226insTTTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.33+132_33+133insTTTG MANE Select | ENSP00000370839.6:n.33+132_33+133insTTTG | |
ENST00000381431.9:c.33+132_33+133insTTTG | ENSP00000370839.5:n.33+132_33+133insTTTG | |
ENST00000506357.5:c.19+132_19+133insTTTG | ||
NM_000232.4:c.33+132_33+133insTTTG , LRG_204t1:c.33+132_33+133insTTTG | NP_000223.1:n.33+132_33+133insTTTG | |
XM_011534403.1:c.33+132_33+133insTTTG | XP_011532705.1:n.33+132_33+133insTTTG | |
NM_000232.5:c.33+132_33+133insTTTG MANE Select | NP_000223.1:n.33+132_33+133insTTTG |