HGVS | Genome Assembly |
---|---|
NC_000009.12:g.12695536_12695541delinsTAAGTA , CM000671.2:g.12695536_12695541delinsTAAGTA | GRCh38 |
NC_000009.11:g.12695536_12695541delinsTAAGTA , CM000671.1:g.12695536_12695541delinsTAAGTA | GRCh37 |
NC_000009.10:g.12685536_12685541delinsTAAGTA | NCBI36 |
NG_011705.1:g.7151_7156delinsTAAGTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000388918.10:c.407_412delinsTAAGTA MANE Select | ENSP00000373570.4:p.Leu136= | |
ENST00000388918.9:c.407_412delinsTAAGTA | ENSP00000373570.4:p.Leu136= | |
NM_000550.2:c.407_412delinsTAAGTA | NP_000541.1:p.Leu136= | |
XR_001746372.2:n.596_601delinsTAAGTA | ||
NM_000550.3:c.407_412delinsTAAGTA MANE Select | NP_000541.1:p.Leu136= |