HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133256145_133256146delinsAG , CM000671.2:g.133256145_133256146delinsAG | GRCh38 |
NC_000009.11:g.136131532_136131533delinsAG , CM000671.1:g.136131532_136131533delinsAG | GRCh37 |
NC_000009.10:g.135121353_135121354delinsAG | NCBI36 |
NG_006669.1:g.21522_21523delinsCT | |
NG_006669.2:g.24070_24071delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.614_615delinsCT | ||
ENST00000647353.1:n.54-4994_54-4993delinsCT | ||
ENST00000651471.1:n.540_541delinsCT | ||
ENST00000679909.1:c.28+19016_28+19017delinsCT | ENSP00000506089.1:n.28+19016_28+19017delinsCT | |
ENST00000453660.3:n.596_597delinsCT | ||
ENST00000538324.2:c.582_583delinsCT | ENSP00000483018.1:p.Phe194= | |
ENST00000611156.4:c.582_583delinsCT | ENSP00000483265.1:p.Phe194= | |
NM_020469.2:c.585_586delinsCT | NP_065202.2:p.Phe195= | |
NM_020469.3:c.585_586delinsCT | NP_065202.2:p.Phe195= |