HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038097_52038098insA , CM000666.2:g.52038097_52038098insA | GRCh38 |
NC_000004.11:g.52904263_52904264insA , CM000666.1:g.52904263_52904264insA | GRCh37 |
NC_000004.10:g.52599020_52599021insA | NCBI36 |
NG_008891.1:g.5222_5223insT , LRG_204:g.5222_5223insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.33+129_33+130insT MANE Select | ENSP00000370839.6:n.33+129_33+130insT | |
ENST00000381431.9:c.33+129_33+130insT | ENSP00000370839.5:n.33+129_33+130insT | |
ENST00000506357.5:c.19+129_19+130insT | ||
NM_000232.4:c.33+129_33+130insT , LRG_204t1:c.33+129_33+130insT | NP_000223.1:n.33+129_33+130insT | |
XM_011534403.1:c.33+129_33+130insT | XP_011532705.1:n.33+129_33+130insT | |
NM_000232.5:c.33+129_33+130insT MANE Select | NP_000223.1:n.33+129_33+130insT |