HGVS | Genome Assembly |
---|---|
NC_000009.12:g.78304839_78304840delinsCT , CM000671.2:g.78304839_78304840delinsCT | GRCh38 |
NC_000009.11:g.80919755_80919756delinsCT , CM000671.1:g.80919755_80919756delinsCT | GRCh37 |
NC_000009.10:g.80109575_80109576delinsCT | NCBI36 |
NG_012165.1:g.12697_12698delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376588.4:c.296_297delinsCT MANE Select | ENSP00000365773.3:p.Ala99= | |
ENST00000347159.6:c.296_297delinsCT | ENSP00000317606.2:p.Ala99= | |
ENST00000376588.3:c.296_297delinsCT | ENSP00000365773.3:p.Ala99= | |
NM_021154.4:c.296_297delinsCT | NP_066977.1:p.Ala99= | |
NM_058179.3:c.296_297delinsCT | NP_478059.1:p.Ala99= | |
NM_058179.4:c.296_297delinsCT MANE Select | NP_478059.1:p.Ala99= | |
NM_021154.5:c.296_297delinsCT | NP_066977.1:p.Ala99= |