HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322971del , CM000677.2:g.73322971del | GRCh38 |
NC_000015.9:g.73615312del , CM000677.1:g.73615312del | GRCh37 |
NC_000015.8:g.71402365del | NCBI36 |
NG_009063.1:g.51297del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261917.4:c.3125del MANE Select | ENSP00000261917.3:p.Pro1042ArgfsTer? | |
ENST00000261917.3:c.3125del | ENSP00000261917.3:p.Pro1042ArgfsTer? | |
NM_005477.2:c.3125del | NP_005468.1:p.Pro1042ArgfsTer? | |
XM_011521148.1:c.1907del | XP_011519450.1:p.Pro636ArgfsTer? | |
XM_011521148.2:c.1907del | XP_011519450.1:p.Pro636ArgfsTer? | |
NM_005477.3:c.3125del MANE Select | NP_005468.1:p.Pro1042ArgfsTer? |