HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322915_73322916del , CM000677.2:g.73322915_73322916del | GRCh38 |
NC_000015.9:g.73615256_73615257del , CM000677.1:g.73615256_73615257del | GRCh37 |
NC_000015.8:g.71402309_71402310del | NCBI36 |
NG_009063.1:g.51353_51354del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.3181_3182del MANE Select | ENSP00000261917.3:p.Pro1061ThrfsTer? | |
ENST00000261917.3:c.3181_3182del | ENSP00000261917.3:p.Pro1061ThrfsTer? | |
NM_005477.2:c.3181_3182del | NP_005468.1:p.Pro1061ThrfsTer? | |
XM_011521148.1:c.1963_1964del | XP_011519450.1:p.Pro655ThrfsTer? | |
XM_011521148.2:c.1963_1964del | XP_011519450.1:p.Pro655ThrfsTer? | |
NM_005477.3:c.3181_3182del MANE Select | NP_005468.1:p.Pro1061ThrfsTer? |