HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320469_159320472del , CM000667.2:g.159320469_159320472del | GRCh38 |
NC_000005.9:g.158747477_158747480del , CM000667.1:g.158747477_158747480del | GRCh37 |
NC_000005.8:g.158680055_158680058del | NCBI36 |
NG_009618.1:g.15006_15009del , LRG_71:g.15006_15009del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.-96_-93del | ENSP00000512849.1:n.-96_-93del | |
ENST00000696751.1:c.*30_*33del | ENSP00000512850.1:n.*30_*33del | |
ENST00000231228.3:c.535_538del MANE Select | ENSP00000231228.2:p.Arg179SerfsTer? | |
ENST00000231228.2:c.535_538del | ENSP00000231228.2:p.Arg179SerfsTer? | |
NM_002187.2:c.535_538del , LRG_71t1:c.535_538del | NP_002178.2:p.Arg179SerfsTer? | |
XR_001742945.1:n.20_23del | ||
NM_002187.3:c.535_538del MANE Select | NP_002178.2:p.Arg179SerfsTer? |