HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038079_52038080delinsCG , CM000666.2:g.52038079_52038080delinsCG | GRCh38 |
NC_000004.11:g.52904245_52904246delinsCG , CM000666.1:g.52904245_52904246delinsCG | GRCh37 |
NC_000004.10:g.52599002_52599003delinsCG | NCBI36 |
NG_008891.1:g.5240_5241delinsCG , LRG_204:g.5240_5241delinsCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.10:c.33+147_33+148delinsCG MANE Select | ENSP00000370839.6:n.33+147_33+148delinsCG | |
ENST00000381431.9:c.33+147_33+148delinsCG | ENSP00000370839.5:n.33+147_33+148delinsCG | |
ENST00000506357.5:c.19+147_19+148delinsCG | ||
NM_000232.4:c.33+147_33+148delinsCG , LRG_204t1:c.33+147_33+148delinsCG | NP_000223.1:n.33+147_33+148delinsCG | |
XM_011534403.1:c.33+147_33+148delinsCG | XP_011532705.1:n.33+147_33+148delinsCG | |
NM_000232.5:c.33+147_33+148delinsCG MANE Select | NP_000223.1:n.33+147_33+148delinsCG |