HGVS | Genome Assembly |
---|---|
NC_000001.11:g.209629891del , CM000663.2:g.209629891del | GRCh38 |
NC_000001.10:g.209803236del , CM000663.1:g.209803236del | GRCh37 |
NC_000001.9:g.207869859del | NCBI36 |
NG_007116.1:g.27585del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356082.9:c.978del MANE Select | ENSP00000348384.3:p.Phe327LeufsTer? | |
ENST00000356082.8:c.978del | ENSP00000348384.3:p.Phe327LeufsTer? | |
ENST00000367030.7:c.978del | ENSP00000355997.3:p.Phe327LeufsTer? | |
ENST00000391911.5:c.978del | ENSP00000375778.1:p.Phe327LeufsTer? | |
NM_000228.2:c.978del | NP_000219.2:p.Phe327LeufsTer? | |
NM_001017402.1:c.978del | NP_001017402.1:p.Phe327LeufsTer? | |
NM_001127641.1:c.978del | NP_001121113.1:p.Phe327LeufsTer? | |
XM_005273124.3:c.978del | XP_005273181.1:p.Phe327LeufsTer? | |
XM_005273124.4:c.978del | XP_005273181.1:p.Phe327LeufsTer? | |
XM_017001272.2:c.786del | XP_016856761.1:p.Phe263LeufsTer? | |
NM_000228.3:c.978del MANE Select | NP_000219.2:p.Phe327LeufsTer? | |
NM_001017402.2:c.978del | NP_001017402.1:p.Phe327LeufsTer? |