HGVS | Genome Assembly |
---|---|
NC_000003.12:g.172448359_172448360delinsCT , CM000665.2:g.172448359_172448360delinsCT | GRCh38 |
NC_000003.11:g.172166149_172166150delinsCT , CM000665.1:g.172166149_172166150delinsCT | GRCh37 |
NC_000003.10:g.173648843_173648844delinsCT | NCBI36 |
NG_021159.1:g.5097_5098delinsAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000241256.3:c.54_55delinsAG MANE Select | ENSP00000241256.2:p.Asp18_Leu19delinsGluV... | |
ENST00000241256.2:c.54_55delinsAG | ENSP00000241256.2:p.Asp18_Leu19delinsGluV... | |
ENST00000427970.1:c.54_55delinsAG | ENSP00000395344.1:p.Asp18_Leu19delinsGluV... | |
NM_004122.2:c.54_55delinsAG | NP_004113.1:p.Asp18_Leu19delinsGluVal | |
NM_198407.2:c.54_55delinsAG MANE Select | NP_940799.1:p.Asp18_Leu19delinsGluVal |