HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133256111_133256112delinsAG , CM000671.2:g.133256111_133256112delinsAG | GRCh38 |
NC_000009.11:g.136131498_136131499delinsAG , CM000671.1:g.136131498_136131499delinsAG | GRCh37 |
NC_000009.10:g.135121319_135121320delinsAG | NCBI36 |
NG_006669.1:g.21556_21557delinsCT | |
NG_006669.2:g.24104_24105delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.648_649delinsCT | ||
ENST00000647353.1:n.54-4960_54-4959delinsCT | ||
ENST00000651471.1:n.574_575delinsCT | ||
ENST00000679909.1:c.28+19050_28+19051delinsCT | ENSP00000506089.1:n.28+19050_28+19051delinsCT | |
ENST00000453660.3:n.630_631delinsCT | ||
ENST00000538324.2:c.616_617delinsCT | ENSP00000483018.1:p.Leu206= | |
ENST00000611156.4:c.616_617delinsCT | ENSP00000483265.1:p.Leu206= | |
NM_020469.2:c.619_620delinsCT | NP_065202.2:p.Leu207= | |
NM_020469.3:c.619_620delinsCT | NP_065202.2:p.Leu207= |