HGVS | Genome Assembly |
---|---|
NC_000017.11:g.29495710_29495712del , CM000679.2:g.29495710_29495712del | GRCh38 |
NC_000017.10:g.27822728_27822730del , CM000679.1:g.27822728_27822730del | GRCh37 |
NC_000017.9:g.24846854_24846856del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261716.8:c.982_984del MANE Select | ENSP00000261716.3:p.Ala328del | |
ENST00000261716.7:c.982_984del | ENSP00000261716.3:p.Ala328del | |
ENST00000536202.1:c.982_984del | ENSP00000438819.1:p.Ala328del | |
ENST00000577583.1:n.830_832del | ||
NM_020791.2:c.982_984del | NP_065842.1:p.Ala328del | |
NM_025142.1:c.982_984del | NP_079418.1:p.Ala328del | |
XM_011525060.1:c.982_984del | XP_011523362.1:p.Ala328del | |
XM_011525060.2:c.982_984del | XP_011523362.1:p.Ala328del | |
NM_020791.4:c.982_984del MANE Select | NP_065842.1:p.Ala328del |