HGVS | Genome Assembly |
---|---|
NC_000019.10:g.49636359_49636361delinsAAG , CM000681.2:g.49636359_49636361delinsAAG | GRCh38 |
NC_000019.9:g.50139616_50139618delinsAAG , CM000681.1:g.50139616_50139618delinsAAG | GRCh37 |
NC_000019.8:g.54831428_54831430delinsAAG | NCBI36 |
NG_042222.1:g.8783_8785delinsCTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000246792.4:c.453+258_453+260delinsCTT MANE Select | ENSP00000246792.2:n.453+258_453+260delinsCTT | |
ENST00000246792.3:c.453+258_453+260delinsCTT | ENSP00000246792.2:n.453+258_453+260delinsCTT | |
ENST00000601532.1:n.593+258_593+260delinsCTT | ||
NM_006270.3:c.453+258_453+260delinsCTT | NP_006261.1:n.453+258_453+260delinsCTT | |
NM_006270.4:c.453+258_453+260delinsCTT | NP_006261.1:n.453+258_453+260delinsCTT | |
NM_006270.5:c.453+258_453+260delinsCTT MANE Select | NP_006261.1:n.453+258_453+260delinsCTT |