HGVS | Genome Assembly |
---|---|
NC_000009.12:g.78329923_78329928delinsTTAAAC , CM000671.2:g.78329923_78329928delinsTTAAAC | GRCh38 |
NC_000009.11:g.80944839_80944844delinsTTAAAC , CM000671.1:g.80944839_80944844delinsTTAAAC | GRCh37 |
NC_000009.10:g.80134659_80134664delinsTTAAAC | NCBI36 |
NG_012165.1:g.37781_37786delinsTTAAAC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376588.4:c.*837_*842delinsTTAAAC MANE Select | ENSP00000365773.3:n.*837_*842delinsTTAAAC... | |
ENST00000376588.3:c.*837_*842delinsTTAAAC | ENSP00000365773.3:n.*837_*842delinsTTAAAC... | |
NM_021154.4:c.*837_*842delinsTTAAAC | NP_066977.1:n.*837_*842delinsTTAAAC | |
NM_058179.3:c.*837_*842delinsTTAAAC | NP_478059.1:n.*837_*842delinsTTAAAC | |
NM_058179.4:c.*837_*842delinsTTAAAC MANE Select | NP_478059.1:n.*837_*842delinsTTAAAC | |
NM_021154.5:c.*837_*842delinsTTAAAC | NP_066977.1:n.*837_*842delinsTTAAAC |