HGVS | Genome Assembly |
---|---|
NC_000011.10:g.55811903_55811904delinsTC , CM000673.2:g.55811903_55811904delinsTC | GRCh38 |
NC_000011.9:g.55579379_55579380delinsTC , CM000673.1:g.55579379_55579380delinsTC | GRCh37 |
NC_000011.8:g.55335955_55335956delinsTC | NCBI36 |
NG_052620.1:g.5537_5538delinsTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000625203.2:c.437_438delinsTC MANE Select | ENSP00000485319.1:p.Ser146Phe | |
ENST00000333973.3:c.437_438delinsTC | ENSP00000335529.2:p.Ser146Phe | |
ENST00000623450.1:c.437_438delinsTC | ENSP00000485509.1:p.Ser146Phe | |
ENST00000625203.1:c.437_438delinsTC | ENSP00000485319.1:p.Ser146Phe | |
NM_001004738.1:c.437_438delinsTC | NP_001004738.1:p.Ser146Phe | |
NM_001004738.2:c.437_438delinsTC MANE Select | NP_001004738.1:p.Ser146Phe |